Search Results For:
- Agreement Type:
- R&D Funding Agreement
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Agreement title
Effective date
Partner type
Technology
Development stage
Adjuvant Global Health Technology Fund - AN2 Therapeutics, Melioidosis & Tuberculosis Therapeutic (Epetraborole) Global Health Agreement
2021
Funder
Industry
Industry
Drug
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
- Equitable access | Ensuring continuity
- Equitable access | Access plans & principles
- Equitable access | Affordable pricing
- Equitable access | Territory access commitments
- Business model | Regulatory strategy
- Business model | Payment structures
- Protecting & sharing information | Confidentiality
- Protecting & sharing information | Information sharing
- Liability | Representations & warranties
PATH - Aridis, Rotavirus Vaccine Development Agreement
2007
Industry
Product development partnership
Product development partnership
Vaccine
Early clinical (through Phase 2)
- Equitable access | Ensuring continuity
- Equitable access | Access plans & principles
- Equitable access | Affordable pricing
- Equitable access | Territory access commitments
- Business model | Governance
- Business model | Payment structures
- Protecting & sharing information | Confidentiality
- Protecting & sharing information | Information sharing
- Protecting & sharing information | Publication of results
- Intellectual property | License grants
- Intellectual property | Ownership of IP
- Intellectual property | Protection of IP
- Liability | Indemnification & liability
- Liability | Insurance
- Liability | Representations & warranties
- Term & termination | Effects of termination
- Term & termination | Term of agreement
- Term & termination | Termination & withdrawal
AXA Prime Impact Master Fund - Revelation Biosciences, Diagnostics & Therapeutics for Viral Infections, Global Health Agreement
2020
Funder
Industry
Industry
Diagnostic
Drug
Drug
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Late clinical (Phase 3)
Commercialization
- Equitable access | Ensuring continuity
- Equitable access | Access plans & principles
- Equitable access | Affordable pricing
- Equitable access | Territory access commitments
- Business model | Product supply
- Protecting & sharing information | Information sharing
- Intellectual property | License grants
- Term & termination | Term of agreement
Gates Foundation - Arsanis RSV Monoclonal Antibodies Funding Agreement
2017
Funder
Industry
Industry
Drug
Preclinical
- Equitable access | Ensuring continuity
- Equitable access | Access plans & principles
- Business model | Payment structures
- Protecting & sharing information | Confidentiality
- Protecting & sharing information | Information sharing
- Protecting & sharing information | Publication of results
- Intellectual property | License grants
- Liability | Indemnification & liability
- Liability | Insurance
- Liability | Representations & warranties
- Term & termination | Effects of termination
- Term & termination | Term of agreement
- Term & termination | Termination & withdrawal
Gates Foundation - Arsanis, S. Aureus Antibody Strategic Relationship Letter Agreement
2017
Funder
Industry
Industry
Drug
Discovery/Concept
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
- Equitable access | Ensuring continuity
- Equitable access | Access plans & principles
- Equitable access | Affordable pricing
- Equitable access | Territory access commitments
- Business model | Governance
- Protecting & sharing information | Confidentiality
- Protecting & sharing information | Information sharing
- Protecting & sharing information | Publication of results
- Intellectual property | License grants
- Liability | Indemnification & liability
- Liability | Representations & warranties
- Term & termination | Effects of termination
- Term & termination | Termination & withdrawal
Gates Foundation - CureVac, Global Access Commitments Agreement
2015
Funder
Industry
Industry
Drug
Vaccine
Vaccine
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Field Testing
Late clinical (Phase 3)
Commercialization
Field Testing
- Equitable access | Ensuring continuity
- Equitable access | Access plans & principles
- Equitable access | Affordable pricing
- Equitable access | Territory access commitments
- Business model | Governance
- Business model | Payment structures
- Protecting & sharing information | Confidentiality
- Protecting & sharing information | Information sharing
- Protecting & sharing information | Publication of results
- Intellectual property | Ownership of IP
- Intellectual property | Protection of IP
- Liability | Indemnification & liability
- Liability | Insurance
- Liability | Representations & warranties
- Term & termination | Term of agreement
- Term & termination | Termination & withdrawal
Gates Foundation - CureVac - GSK, Letter Agreement for Alignment on Global Access Commitments
2020
Funder
Industry
Industry
Drug
Vaccine
Vaccine
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
- Equitable access | Ensuring continuity
- Equitable access | Access plans & principles
- Protecting & sharing information | Confidentiality
- Protecting & sharing information | Information sharing
- Protecting & sharing information | Publication of results
- Intellectual property | License grants
- Intellectual property | Ownership of IP
- Liability | Representations & warranties
- Term & termination | Term of agreement
Gates Foundation - Icosavax, COVID-19 Vaccine Global Access and Price Commitments Agreement
2021
Funder
Industry
Industry
Vaccine
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Late clinical (Phase 3)
Commercialization
- Equitable access | Ensuring continuity
- Equitable access | Access plans & principles
- Equitable access | Affordable pricing
- Equitable access | Territory access commitments
- Business model | Product supply
- Protecting & sharing information | Publication of results
- Intellectual property | License grants
- Intellectual property | Ownership of IP
- Liability | Representations & warranties
CARB-X Portfolio Company Agreement Template
2019
Academic institution
Funder
Industry
Non-profit research organization
Product development partnership
Funder
Industry
Non-profit research organization
Product development partnership
Diagnostic
Drug
Drug
Discovery/Concept
Preclinical
Early clinical (through Phase 2)
Preclinical
Early clinical (through Phase 2)
- Equitable access | Ensuring continuity
- Equitable access | Access plans & principles
- Equitable access | Territory access commitments
- Business model | Clinical trial conduct
- Business model | Quality management
- Business model | Regulatory strategy
- Business model | Governance
- Business model | Payment structures
- Protecting & sharing information | Confidentiality
- Protecting & sharing information | Information sharing
- Protecting & sharing information | Publication of results
- Intellectual property | Ownership of IP
- Liability | Indemnification & liability
- Liability | Insurance
- Liability | Representations & warranties
- Term & termination | Effects of termination
- Term & termination | Termination & withdrawal
CEPI CfP3i Vaccine Funding Agreement Template
2018
Funder
Industry
Industry
Vaccine
Preclinical
Early clinical (through Phase 2)
Early clinical (through Phase 2)
- Equitable access | Ensuring continuity
- Equitable access | Access plans & principles
- Equitable access | Preparedness & response
- Equitable access | Territory access commitments
- Business model | Benefit sharing
- Business model | Clinical trial conduct
- Business model | Quality management
- Business model | Regulatory strategy
- Business model | Governance
- Business model | Payment structures
- Protecting & sharing information | Confidentiality
- Protecting & sharing information | Information sharing
- Protecting & sharing information | Publication of results
- Protecting & sharing information | Technology transfer
- Intellectual property | License grants
- Intellectual property | Ownership of IP
- Intellectual property | Protection of IP
- Liability | Indemnification & liability
- Liability | Insurance
- Liability | Representations & warranties
- Term & termination | Effects of termination
- Term & termination | Term of agreement
- Term & termination | Termination & withdrawal
CEPI - CureVac, Framework Partnering Agreement
2019
Funder
Industry
Industry
Vaccine
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
- Equitable access | Ensuring continuity
- Equitable access | Access plans & principles
- Equitable access | Preparedness & response
- Equitable access | Affordable pricing
- Equitable access | Territory access commitments
- Business model | Benefit sharing
- Business model | Clinical trial conduct
- Business model | Quality management
- Business model | Regulatory strategy
- Business model | Governance
- Business model | Payment structures
- Protecting & sharing information | Confidentiality
- Protecting & sharing information | Information sharing
- Protecting & sharing information | Publication of results
- Protecting & sharing information | Technology transfer
- Intellectual property | License grants
- Intellectual property | Ownership of IP
- Intellectual property | Protection of IP
- Liability | Indemnification & liability
- Liability | Insurance
- Liability | Representations & warranties
- Term & termination | Effects of termination
- Term & termination | Term of agreement
- Term & termination | Termination & withdrawal
CEPI - University of Oxford - Barinthus Biotherapeutics, ChAdOx1 MERS Vaccine R&D Funding Agreement
2023
Academic institution
Funder
Industry
Funder
Industry
Vaccine
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
- Equitable access | Ensuring continuity
- Equitable access | Access plans & principles
- Equitable access | Preparedness & response
- Equitable access | Territory access commitments
- Business model | Benefit sharing
- Business model | Regulatory strategy
- Business model | Governance
- Business model | Payment structures
- Business model | Product supply
- Protecting & sharing information | Confidentiality
- Protecting & sharing information | Information sharing
- Protecting & sharing information | Publication of results
- Protecting & sharing information | Technology transfer
- Intellectual property | License grants
- Intellectual property | Ownership of IP
- Intellectual property | Protection of IP
- Liability | Indemnification & liability
- Liability | Insurance
- Liability | Representations & warranties
- Term & termination | Effects of termination
- Term & termination | Term of agreement
- Term & termination | Termination & withdrawal
CEPI - Valneva, Chikungunya Vaccine Funding Agreement
2019
Funder
Industry
Industry
Vaccine
Preclinical
Early clinical (through Phase 2)
Early clinical (through Phase 2)
- Equitable access | Ensuring continuity
- Equitable access | Access plans & principles
- Equitable access | Preparedness & response
- Equitable access | Affordable pricing
- Equitable access | Territory access commitments
- Business model | Benefit sharing
- Business model | Clinical trial conduct
- Business model | Quality management
- Business model | Regulatory strategy
- Business model | Governance
- Business model | Payment structures
- Protecting & sharing information | Confidentiality
- Protecting & sharing information | Information sharing
- Protecting & sharing information | Publication of results
- Protecting & sharing information | Technology transfer
- Intellectual property | License grants
- Intellectual property | Ownership of IP
- Intellectual property | Protection of IP
- Liability | Indemnification & liability
- Liability | Insurance
- Liability | Representations & warranties
- Term & termination | Effects of termination
- Term & termination | Term of agreement
- Term & termination | Termination & withdrawal
CEPI - VBI, COVID-19 Vaccine Development Funding Agreement
2021
Funder
Industry
Industry
Vaccine
Preclinical
Early clinical (through Phase 2)
Early clinical (through Phase 2)
- Equitable access | Ensuring continuity
- Equitable access | Access plans & principles
- Equitable access | Preparedness & response
- Equitable access | Affordable pricing
- Equitable access | Territory access commitments
- Business model | Benefit sharing
- Business model | Clinical trial conduct
- Business model | Regulatory strategy
- Business model | Governance
- Business model | Payment structures
- Business model | Product supply
- Protecting & sharing information | Confidentiality
- Protecting & sharing information | Information sharing
- Protecting & sharing information | Publication of results
- Intellectual property | License grants
- Intellectual property | Ownership of IP
- Intellectual property | Protection of IP
- Liability | Indemnification & liability
- Liability | Insurance
- Liability | Representations & warranties
- Term & termination | Effects of termination
- Term & termination | Term of agreement
- Term & termination | Termination & withdrawal
FIND Sample Funding Terms and Conditions
2021
Academic institution
Industry
Product development partnership
Industry
Product development partnership
Diagnostic
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
- Equitable access | Access plans & principles
- Equitable access | Affordable pricing
- Equitable access | Territory access commitments
- Business model | Quality management
- Business model | Regulatory strategy
- Business model | Governance
- Protecting & sharing information | Publication of results
- Protecting & sharing information | Technology transfer
- Intellectual property | License grants
- Liability | Indemnification & liability
- Liability | Representations & warranties
Funder Development Partnering Agreement Template
2018
Funder
Industry
Non-profit research organization
Product development partnership
Industry
Non-profit research organization
Product development partnership
Device
Diagnostic
Drug
Vaccine
Diagnostic
Drug
Vaccine
Discovery/Concept
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Field Testing
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Field Testing
- Equitable access | Ensuring continuity
- Equitable access | Access plans & principles
- Equitable access | Preparedness & response
- Equitable access | Affordable pricing
- Equitable access | Territory access commitments
- Business model | Benefit sharing
- Business model | Clinical trial conduct
- Business model | Quality management
- Business model | Regulatory strategy
- Business model | Governance
- Business model | Payment structures
- Protecting & sharing information | Confidentiality
- Protecting & sharing information | Information sharing
- Protecting & sharing information | Publication of results
- Intellectual property | License grants
- Intellectual property | Ownership of IP
- Intellectual property | Protection of IP
- Liability | Indemnification & liability
- Liability | Insurance
- Liability | Representations & warranties
- Term & termination | Effects of termination
- Term & termination | Term of agreement
- Term & termination | Termination & withdrawal
Gates Foundation - Amyris, Inc., Malaria Therapeutic (artemisinin-based combination therapies - ACTs), Letter Agreement
2016
Funder
Industry
Industry
Drug
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Late clinical (Phase 3)
Commercialization
- Equitable access | Ensuring continuity
- Equitable access | Access plans & principles
- Equitable access | Affordable pricing
- Equitable access | Territory access commitments
- Business model | Governance
- Business model | Product supply
- Protecting & sharing information | Confidentiality
- Protecting & sharing information | Information sharing
- Protecting & sharing information | Technology transfer
- Intellectual property | License grants
- Intellectual property | Protection of IP
- Liability | Indemnification & liability
- Liability | Representations & warranties
- Term & termination | Effects of termination
- Term & termination | Termination & withdrawal
Gates Foundation - BioNTech, TB & HIV Product Strategic Letter Agreement
2019
Funder
Industry
Industry
Drug
Vaccine
Vaccine
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
- Equitable access | Ensuring continuity
- Equitable access | Access plans & principles
- Equitable access | Preparedness & response
- Equitable access | Affordable pricing
- Equitable access | Territory access commitments
- Business model | Governance
- Protecting & sharing information | Confidentiality
- Protecting & sharing information | Information sharing
- Protecting & sharing information | Publication of results
- Intellectual property | License grants
- Liability | Indemnification & liability
- Liability | Insurance
- Term & termination | Effects of termination
- Term & termination | Termination & withdrawal
Gates Foundation - Icosavax, COVID-19 Vaccine Grant Agreement
2021
Funder
Industry
Industry
Vaccine
Early clinical (through Phase 2)
Late clinical (Phase 3)
Late clinical (Phase 3)
- Equitable access | Ensuring continuity
- Equitable access | Access plans & principles
- Business model | Payment structures
- Protecting & sharing information | Confidentiality
- Protecting & sharing information | Information sharing
- Protecting & sharing information | Publication of results
- Intellectual property | License grants
- Liability | Indemnification & liability
- Liability | Insurance
- Liability | Representations & warranties
- Term & termination | Effects of termination
- Term & termination | Term of agreement
- Term & termination | Termination & withdrawal
Gates Foundation - Novavax, RSV Vaccine Global Access Commitments Agreement
2015
Funder
Industry
Industry
Vaccine
Late clinical (Phase 3)
Commercialization
Commercialization
- Equitable access | Ensuring continuity
- Equitable access | Access plans & principles
- Equitable access | Affordable pricing
- Equitable access | Territory access commitments
- Business model | Governance
- Protecting & sharing information | Confidentiality
- Protecting & sharing information | Information sharing
- Protecting & sharing information | Publication of results
- Protecting & sharing information | Technology transfer
- Liability | Indemnification & liability
- Liability | Representations & warranties
- Term & termination | Effects of termination
- Term & termination | Term of agreement
Gates Foundation Sample Grant Terms & Conditions
2019
Academic institution
Funder
Industry
Product development partnership
Funder
Industry
Product development partnership
Device
Diagnostic
Drug
Vaccine
Diagnostic
Drug
Vaccine
Discovery/Concept
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Field Testing
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Field Testing
Gates Foundation - Visterra, Strategic Relationship Letter Agreement
2012
Funder
Industry
Industry
Drug
Vaccine
Vaccine
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
- Equitable access | Ensuring continuity
- Equitable access | Access plans & principles
- Equitable access | Territory access commitments
- Business model | Governance
- Protecting & sharing information | Confidentiality
- Protecting & sharing information | Information sharing
- Intellectual property | License grants
- Liability | Indemnification & liability
- Term & termination | Effects of termination
- Term & termination | Termination & withdrawal
IMI 1 Model Grant Agreement
2011
Academic institution
Funder
Industry
Non-profit research organization
Product development partnership
Funder
Industry
Non-profit research organization
Product development partnership
Device
Diagnostic
Drug
Vaccine
Diagnostic
Drug
Vaccine
Discovery/Concept
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Field Testing
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Field Testing
IMI 2 Model Grant Agreement
2017
Academic institution
Funder
Industry
Non-profit research organization
Product development partnership
Funder
Industry
Non-profit research organization
Product development partnership
Device
Diagnostic
Drug
Vaccine
Diagnostic
Drug
Vaccine
Discovery/Concept
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Field Testing
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Field Testing
- Equitable access | Ensuring continuity
- Protecting & sharing information | Confidentiality
- Protecting & sharing information | Publication of results
- Intellectual property | License grants
- Intellectual property | Ownership of IP
- Intellectual property | Protection of IP
- Liability | Indemnification & liability
India Department of Biotechnology (DBT), Memorandum of Agreement
2023
Academic institution
Government
Government
Device
Diagnostic
Drug
Vaccine
Diagnostic
Drug
Vaccine
Discovery/Concept
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
- Equitable access | Ensuring continuity
- Equitable access | Access plans & principles
- Business model | Governance
- Business model | Payment structures
- Protecting & sharing information | Information sharing
- Protecting & sharing information | Publication of results
- Intellectual property | Ownership of IP
- Intellectual property | Protection of IP
- Term & termination | Effects of termination
- Term & termination | Term of agreement
- Term & termination | Termination & withdrawal
BARDA - Moderna, COVID-19 Vaccine Development Agreement
2020
Government
Industry
Industry
Vaccine
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Early clinical (through Phase 2)
Late clinical (Phase 3)
- Equitable access | Ensuring continuity
- Business model | Governance
- Protecting & sharing information | Confidentiality
- Protecting & sharing information | Information sharing
- Intellectual property | License grants
- Intellectual property | Ownership of IP
- Intellectual property | Protection of IP
- Liability | Indemnification & liability
MPP – Afrigen Biologics, COVID-19 mRNA-Based Vaccines and Therapeutics, Grant Agreement
2022
Industry
Multilateral organization
Multilateral organization
Drug
Vaccine
Vaccine
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
- Equitable access | Ensuring continuity
- Business model | Governance
- Business model | Payment structures
- Protecting & sharing information | Confidentiality
- Protecting & sharing information | Information sharing
- Protecting & sharing information | Publication of results
- Intellectual property | License grants
- Intellectual property | Ownership of IP
- Intellectual property | Protection of IP
- Liability | Indemnification & liability
- Liability | Insurance
- Liability | Representations & warranties
- Term & termination | Effects of termination
- Term & termination | Term of agreement
- Term & termination | Termination & withdrawal
MPP – Afrigen Biologics, RSV mRNA-Based Vaccine, Grant Agreement
2023
Industry
Multilateral organization
Multilateral organization
Vaccine
Discovery/Concept
Preclinical
Early clinical (through Phase 2)
Preclinical
Early clinical (through Phase 2)
- Business model | Governance
- Business model | Payment structures
- Protecting & sharing information | Confidentiality
- Protecting & sharing information | Information sharing
- Protecting & sharing information | Publication of results
- Intellectual property | License grants
- Intellectual property | Ownership of IP
- Intellectual property | Protection of IP
- Liability | Indemnification & liability
- Liability | Insurance
- Liability | Representations & warranties
- Term & termination | Effects of termination
- Term & termination | Term of agreement
- Term & termination | Termination & withdrawal
MPP - Biovac, mRNA Vaccine Technology Transfer Agreement
2024
Industry
Multilateral organization
Multilateral organization
Vaccine
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Late clinical (Phase 3)
Commercialization
- Equitable access | Access plans & principles
- Equitable access | Preparedness & response
- Equitable access | Affordable pricing
- Equitable access | Territory access commitments
- Business model | Governance
- Business model | Payment structures
- Protecting & sharing information | Confidentiality
- Protecting & sharing information | Information sharing
- Protecting & sharing information | Technology transfer
- Intellectual property | License grants
- Liability | Indemnification & liability
- Liability | Representations & warranties
- Term & termination | Effects of termination
- Term & termination | Term of agreement
- Term & termination | Termination & withdrawal
MPP – South African Medical Research Council, COVID-19 mRNA-Based Vaccines and Therapeutics, Grant Agreement
2022
Government
Multilateral organization
Multilateral organization
Drug
Vaccine
Vaccine
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
- Equitable access | Ensuring continuity
- Business model | Governance
- Business model | Payment structures
- Protecting & sharing information | Confidentiality
- Protecting & sharing information | Information sharing
- Protecting & sharing information | Publication of results
- Intellectual property | License grants
- Intellectual property | Ownership of IP
- Intellectual property | Protection of IP
- Liability | Indemnification & liability
- Liability | Insurance
- Liability | Representations & warranties
- Term & termination | Effects of termination
- Term & termination | Term of agreement
- Term & termination | Termination & withdrawal
CEPI - Novavax, COVID-19 Vaccine Funding Agreement
2020
Funder
Industry
Industry
Vaccine
Commercialization
- Equitable access | Ensuring continuity
- Equitable access | Access plans & principles
- Equitable access | Preparedness & response
- Equitable access | Affordable pricing
- Equitable access | Territory access commitments
- Business model | Benefit sharing
- Business model | Clinical trial conduct
- Business model | Quality management
- Business model | Regulatory strategy
- Business model | Governance
- Business model | Payment structures
- Business model | Product supply
- Protecting & sharing information | Confidentiality
- Protecting & sharing information | Information sharing
- Protecting & sharing information | Publication of results
- Intellectual property | License grants
- Intellectual property | Ownership of IP
- Intellectual property | Protection of IP
- Liability | Indemnification & liability
- Liability | Insurance
- Liability | Representations & warranties
- Term & termination | Effects of termination
- Term & termination | Term of agreement
- Term & termination | Termination & withdrawal
US Department of Defense - Novavax, COVID-19 Vaccine Development Agreement
2020
Government
Industry
Industry
Vaccine
Late clinical (Phase 3)
Commercialization
Commercialization
- Equitable access | Ensuring continuity
- Business model | Quality management
- Business model | Regulatory strategy
- Protecting & sharing information | Publication of results
- Intellectual property | License grants
- Intellectual property | Ownership of IP
- Liability | Indemnification & liability
- Liability | Representations & warranties
- Term & termination | Effects of termination
- Term & termination | Term of agreement
- Term & termination | Termination & withdrawal
US Department of Defense – Regeneron, COVID-19 Antibodies Large-Scale Manufacturing Agreement
2020
Government
Industry
Industry
Drug
Late clinical (Phase 3)
Commercialization
Commercialization
- Equitable access | Ensuring continuity
- Business model | Regulatory strategy
- Business model | Payment structures
- Business model | Product supply
- Protecting & sharing information | Information sharing
- Intellectual property | License grants
- Intellectual property | Ownership of IP
- Intellectual property | Protection of IP
- Liability | Indemnification & liability
US Department of Defense - Sanofi, COVID-19 Vaccine Development Agreement
2020
Government
Industry
Industry
Vaccine
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Field Testing
Late clinical (Phase 3)
Commercialization
Field Testing
- Equitable access | Ensuring continuity
- Equitable access | Affordable pricing
- Business model | Quality management
- Business model | Regulatory strategy
- Business model | Governance
- Protecting & sharing information | Confidentiality
- Protecting & sharing information | Publication of results
- Intellectual property | License grants
- Liability | Indemnification & liability
US Department of Defense - Inovio, COVID-19 Vaccine Delivery Device, Other Transaction Prototype Agreement
2020
Government
Industry
Industry
Device
Vaccine
Vaccine
Early clinical (through Phase 2)
Late clinical (Phase 3)
Late clinical (Phase 3)
- Equitable access | Ensuring continuity
- Business model | Quality management
- Business model | Regulatory strategy
- Business model | Governance
- Business model | Payment structures
- Protecting & sharing information | Confidentiality
- Protecting & sharing information | Information sharing
- Protecting & sharing information | Publication of results
- Intellectual property | License grants
- Intellectual property | Ownership of IP
- Intellectual property | Protection of IP
- Liability | Indemnification & liability
- Liability | Representations & warranties
- Term & termination | Effects of termination
- Term & termination | Term of agreement
- Term & termination | Termination & withdrawal
UnitaidExplore Sample Funding Terms and Conditions
2020
Academic institution
Funder
Industry
Product development partnership
Funder
Industry
Product development partnership
Device
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
- Equitable access | Ensuring continuity
- Equitable access | Access plans & principles
- Equitable access | Affordable pricing
- Equitable access | Territory access commitments
- Business model | Governance
- Business model | Payment structures
- Protecting & sharing information | Confidentiality
- Protecting & sharing information | Information sharing
- Protecting & sharing information | Publication of results
- Intellectual property | License grants
- Liability | Indemnification & liability
- Liability | Insurance
- Liability | Representations & warranties
- Term & termination | Effects of termination
- Term & termination | Term of agreement
- Term & termination | Termination & withdrawal
US Department of Defense - Janssen, COVID-19 Vaccine Large Scale Manufacturing Agreement
2020
Government
Industry
Industry
Vaccine
Commercialization
- Equitable access | Ensuring continuity
- Equitable access | Affordable pricing
- Business model | Quality management
- Business model | Regulatory strategy
- Business model | Governance
- Business model | Payment structures
- Business model | Product supply
- Protecting & sharing information | Confidentiality
- Protecting & sharing information | Information sharing
- Protecting & sharing information | Publication of results
- Intellectual property | License grants
- Intellectual property | Ownership of IP
- Intellectual property | Protection of IP
- Liability | Indemnification & liability
- Liability | Representations & warranties
- Term & termination | Effects of termination
- Term & termination | Term of agreement
- Term & termination | Termination & withdrawal
Wellcome Trust - Alto Neuroscience, Bipolar Depression Therapeutic Convertible Loan Agreement
2024
Funder
Industry
Industry
Drug
Early clinical (through Phase 2)
Late clinical (Phase 3)
Late clinical (Phase 3)
- Equitable access | Ensuring continuity
- Equitable access | Access plans & principles
- Business model | Clinical trial conduct
- Business model | Governance
- Business model | Payment structures
- Protecting & sharing information | Confidentiality
- Protecting & sharing information | Information sharing
- Protecting & sharing information | Publication of results
- Intellectual property | Ownership of IP
- Intellectual property | Protection of IP
- Liability | Indemnification & liability
- Liability | Insurance
- Liability | Representations & warranties
- Term & termination | Effects of termination
- Term & termination | Term of agreement
- Term & termination | Termination & withdrawal
Wellcome Trust - PTC Therapeutics, Cancer Treatment Research Funding Agreement
2010
Funder
Industry
Industry
Drug
Discovery/Concept
Preclinical
Preclinical
- Equitable access | Ensuring continuity
- Business model | Regulatory strategy
- Business model | Governance
- Business model | Payment structures
- Protecting & sharing information | Confidentiality
- Protecting & sharing information | Information sharing
- Protecting & sharing information | Publication of results
- Intellectual property | Ownership of IP
- Intellectual property | Protection of IP
- Liability | Indemnification & liability
- Liability | Representations & warranties
- Term & termination | Effects of termination
- Term & termination | Term of agreement
- Term & termination | Termination & withdrawal
Wellcome Trust Standard Grant Terms & Conditions
2021
Academic institution
Funder
Industry
Funder
Industry
Device
Diagnostic
Drug
Vaccine
Diagnostic
Drug
Vaccine
Discovery/Concept
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
- Equitable access | Ensuring continuity
- Equitable access | Access plans & principles
- Business model | Benefit sharing
- Business model | Governance
- Business model | Payment structures
- Protecting & sharing information | Confidentiality
- Protecting & sharing information | Information sharing
- Protecting & sharing information | Publication of results
- Intellectual property | Ownership of IP
- Intellectual property | Protection of IP
- Liability | Indemnification & liability
- Term & termination | Termination & withdrawal
NIH - Fluidigm, COVID-19 Diagnostic Development Agreement
2020
Government
Industry
Industry
Diagnostic
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Late clinical (Phase 3)
Commercialization
- Equitable access | Ensuring continuity
- Equitable access | Affordable pricing
- Business model | Regulatory strategy
- Business model | Governance
- Business model | Payment structures
- Business model | Product supply
- Protecting & sharing information | Confidentiality
- Protecting & sharing information | Information sharing
- Protecting & sharing information | Publication of results
- Intellectual property | License grants
- Intellectual property | Ownership of IP
- Intellectual property | Protection of IP
- Liability | Indemnification & liability
- Term & termination | Effects of termination
- Term & termination | Term of agreement
- Term & termination | Termination & withdrawal
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Should the developer be required to comply with an equitable access policy? Should the developer be required to establish an access plan? 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Are the parties required to meet in accordance with a defined schedule for decision-making and progress reporting activities? What are the resolution mechanisms for disputes related to the agreement? Are there any requirements for policies or procedures to manage potential conflicts of interest? [parent] => 53 [count] => 87 [filter] => raw [parent_name] => Business model [parent_slug] => business-model ) [80] => WP_Term Object ( [term_id] => 80 [name] => Indemnification & liability [slug] => indemnity [term_group] => 0 [term_taxonomy_id] => 80 [taxonomy] => issue [description] => What occurrences could result in a liability claim against which one party will indemnify the other? Are there any circumstances under which one party will not indemnify the other? What is the process for managing liability claims? Are there government or other types of indemnification schemes? Is there any limitation or monetary cap on each party’s liabilities under the agreement? 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What is the scope of the licensed intellectual property? What is the territory of the license? Is the license exclusive or non-exclusive? Are there any restrictions on the use of the licensed intellectual property? Are there any specific obligations to exploit the licensed intellectual property? Can the licensee grant sublicenses to third parties? Will products manufactured under license be marketed as branded or generic? 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[parent] => 53 [count] => 79 [filter] => raw [parent_name] => Business model [parent_slug] => business-model ) [102] => WP_Term Object ( [term_id] => 102 [name] => Preparedness & response [slug] => outbreak-preparedness [term_group] => 0 [term_taxonomy_id] => 102 [taxonomy] => issue [description] => [parent] => 46 [count] => 13 [filter] => raw [parent_name] => Equitable access [parent_slug] => access-to-medicines ) [268] => WP_Term Object ( [term_id] => 268 [name] => Product supply [slug] => supply-purchase-of-products [term_group] => 0 [term_taxonomy_id] => 268 [taxonomy] => issue [description] => [parent] => 53 [count] => 43 [filter] => raw [parent_name] => Business model [parent_slug] => business-model ) [49] => WP_Term Object ( [term_id] => 49 [name] => Protecting & sharing information [slug] => information-sharing [term_group] => 0 [term_taxonomy_id] => 49 [taxonomy] => issue [description] => [parent] => 0 [count] => 0 [filter] => raw [parent_name] => [parent_slug] => ) [90] => WP_Term Object ( [term_id] => 90 [name] => Protection of IP [slug] => protection-results [term_group] => 0 [term_taxonomy_id] => 90 [taxonomy] => issue [description] => [parent] => 48 [count] => 70 [filter] => raw [parent_name] => Intellectual property [parent_slug] => ip-ownership ) [290] => WP_Term Object ( [term_id] => 290 [name] => Publication of results [slug] => publication-of-results [term_group] => 0 [term_taxonomy_id] => 290 [taxonomy] => issue [description] => What information are the parties required or permitted to publish? What is the required timeline for making data available? What are the acceptable publication channels? Is compliance with a specific open access policy required? [parent] => 49 [count] => 61 [filter] => raw [parent_name] => Protecting & sharing information [parent_slug] => information-sharing ) [372] => WP_Term Object ( [term_id] => 372 [name] => Quality management [slug] => quality-management [term_group] => 0 [term_taxonomy_id] => 372 [taxonomy] => issue [description] => [parent] => 53 [count] => 36 [filter] => raw [parent_name] => Business model [parent_slug] => business-model ) [56] => WP_Term Object ( [term_id] => 56 [name] => Regulatory strategy [slug] => regulatory-strategy [term_group] => 0 [term_taxonomy_id] => 56 [taxonomy] => issue [description] => [parent] => 53 [count] => 53 [filter] => raw [parent_name] => Business model [parent_slug] => business-model ) [81] => WP_Term Object ( [term_id] => 81 [name] => Representations & warranties [slug] => warranties [term_group] => 0 [term_taxonomy_id] => 81 [taxonomy] => issue [description] => Should the parties make any warranties, and if so, what is the scope? [parent] => 50 [count] => 88 [filter] => raw [parent_name] => Liability [parent_slug] => liability ) [86] => WP_Term Object ( [term_id] => 86 [name] => Technology transfer [slug] => technology-transfer [term_group] => 0 [term_taxonomy_id] => 86 [taxonomy] => issue [description] => What is included in the technology and/or materials to be transferred? What are the responsibilities of each party to in relation to the transfer of materials and/or technology? [parent] => 49 [count] => 41 [filter] => raw [parent_name] => Protecting & sharing information [parent_slug] => information-sharing ) [52] => WP_Term Object ( [term_id] => 52 [name] => Term & termination [slug] => term-and-termination [term_group] => 0 [term_taxonomy_id] => 52 [taxonomy] => issue [description] => Term What is the term of the agreement? Is it tied to the timeline of the project or license grants? Termination Under what circumstances may a party terminate or withdraw from the agreement? Effects of Termination What are the effects of termination or withdrawal by a party? [parent] => 0 [count] => 0 [filter] => raw [parent_name] => [parent_slug] => ) [76] => WP_Term Object ( [term_id] => 76 [name] => Term of agreement [slug] => term-of-agreement [term_group] => 0 [term_taxonomy_id] => 76 [taxonomy] => issue [description] => [parent] => 52 [count] => 87 [filter] => raw [parent_name] => Term & termination [parent_slug] => term-and-termination ) [74] => WP_Term Object ( [term_id] => 74 [name] => Termination & withdrawal [slug] => termination-and-withdrawal [term_group] => 0 [term_taxonomy_id] => 74 [taxonomy] => issue [description] => [parent] => 52 [count] => 91 [filter] => raw [parent_name] => Term & termination [parent_slug] => term-and-termination ) [282] => WP_Term Object ( [term_id] => 282 [name] => Territory access commitments [slug] => territory-access-commitments [term_group] => 0 [term_taxonomy_id] => 282 [taxonomy] => issue [description] => How should ‘territory’ be defined under the agreement? Should the definition make a distinction between different types of purchaser (e.g. public sector vs. private sector)? Should the developer be required to apply for regulatory approval in priority access markets? Should the developer be required to commit a proportion of the product manufactured to a certain country or purchasing organization? Should the developer be required to identify a third party that could fulfill supply requirements for the access territories in the event that the developer does not? Should the agreement include any anti-diversion provisions? [parent] => 46 [count] => 58 [filter] => raw [parent_name] => Equitable access [parent_slug] => access-to-medicines ) ) [issues_by_slug:GHIAA2019\MapguideSearch:private] => Array ( [equitable-access] => WP_Term Object ( [term_id] => 101 [name] => Access plans & principles [slug] => equitable-access [term_group] => 0 [term_taxonomy_id] => 101 [taxonomy] => issue [description] => How should equitable or global access be defined? Should the developer be required to comply with an equitable access policy? Should the developer be required to establish an access plan? [parent] => 46 [count] => 51 [filter] => raw [parent_name] => Equitable access [parent_slug] => access-to-medicines ) [pricing] => WP_Term Object ( [term_id] => 100 [name] => Affordable pricing [slug] => pricing [term_group] => 0 [term_taxonomy_id] => 100 [taxonomy] => issue [description] => [parent] => 46 [count] => 49 [filter] => raw [parent_name] => Equitable access [parent_slug] => access-to-medicines ) [benefit-revenue-sharing] => WP_Term Object ( [term_id] => 66 [name] => Benefit sharing [slug] => benefit-revenue-sharing [term_group] => 0 [term_taxonomy_id] => 66 [taxonomy] => issue [description] => [parent] => 53 [count] => 15 [filter] => raw [parent_name] => Business model [parent_slug] => business-model ) [business-model] => WP_Term Object ( [term_id] => 53 [name] => Business model [slug] => business-model [term_group] => 0 [term_taxonomy_id] => 53 [taxonomy] => issue [description] => [parent] => 0 [count] => 0 [filter] => raw [parent_name] => [parent_slug] => ) [clinical-trial-conduct] => WP_Term Object ( [term_id] => 371 [name] => Clinical trial conduct [slug] => clinical-trial-conduct [term_group] => 0 [term_taxonomy_id] => 371 [taxonomy] => issue [description] => [parent] => 53 [count] => 15 [filter] => raw [parent_name] => Business model [parent_slug] => business-model ) [confidentiality] => WP_Term Object ( [term_id] => 84 [name] => Confidentiality [slug] => confidentiality [term_group] => 0 [term_taxonomy_id] => 84 [taxonomy] => issue [description] => What is the scope of confidential information? What are the obligations of the parties to protect confidential information? Are there any exceptions to the confidentiality obligations? Are the parties permitted to make public announcements related to the project? Can the parties use each other’s name and logo for general marketing materials? [parent] => 49 [count] => 102 [filter] => raw [parent_name] => Protecting & sharing information [parent_slug] => information-sharing ) [donation] => WP_Term Object ( [term_id] => 271 [name] => Donation [slug] => donation [term_group] => 0 [term_taxonomy_id] => 271 [taxonomy] => issue [description] => [parent] => 46 [count] => 5 [filter] => raw [parent_name] => Equitable access [parent_slug] => access-to-medicines ) [effect-of-termination] => WP_Term Object ( [term_id] => 72 [name] => Effects of termination [slug] => effect-of-termination [term_group] => 0 [term_taxonomy_id] => 72 [taxonomy] => issue [description] => [parent] => 52 [count] => 84 [filter] => raw [parent_name] => Term & termination [parent_slug] => term-and-termination ) [ensuring-continuity] => WP_Term Object ( [term_id] => 281 [name] => Ensuring continuity [slug] => ensuring-continuity [term_group] => 0 [term_taxonomy_id] => 281 [taxonomy] => issue [description] => Under what circumstances can the continuity rights be exercised? (What are the conditions precedent?) What is an appropriate scope for the continuity rights? What are the rights and obligations of each party? Should related license grants vest upon execution of the agreement, or at a later stage in development? Should there be an escrow requirement? Should there be any restrictions on the developer’s ability to transfer project-related intellectual property to a third party? [parent] => 46 [count] => 55 [filter] => raw [parent_name] => Equitable access [parent_slug] => access-to-medicines ) [access-to-medicines] => WP_Term Object ( [term_id] => 46 [name] => Equitable access [slug] => access-to-medicines [term_group] => 0 [term_taxonomy_id] => 46 [taxonomy] => issue [description] => [parent] => 0 [count] => 0 [filter] => raw [parent_name] => [parent_slug] => ) [roles-responsibilities] => WP_Term Object ( [term_id] => 278 [name] => Governance [slug] => roles-responsibilities [term_group] => 0 [term_taxonomy_id] => 278 [taxonomy] => issue [description] => Do the parties govern the project through a joint steering committee ("JSC")? If so, what are the parties expressly designated roles and responsibilities with respect to the JSC? Are there other committees, important governance bodies, or designated individual positions? What are the parties' roles and responsibilities with respect to them? Are the parties required to meet in accordance with a defined schedule for decision-making and progress reporting activities? What are the resolution mechanisms for disputes related to the agreement? Are there any requirements for policies or procedures to manage potential conflicts of interest? [parent] => 53 [count] => 87 [filter] => raw [parent_name] => Business model [parent_slug] => business-model ) [indemnity] => WP_Term Object ( [term_id] => 80 [name] => Indemnification & liability [slug] => indemnity [term_group] => 0 [term_taxonomy_id] => 80 [taxonomy] => issue [description] => What occurrences could result in a liability claim against which one party will indemnify the other? Are there any circumstances under which one party will not indemnify the other? What is the process for managing liability claims? Are there government or other types of indemnification schemes? Is there any limitation or monetary cap on each party’s liabilities under the agreement? [parent] => 50 [count] => 99 [filter] => raw [parent_name] => Liability [parent_slug] => liability ) [information-sharing-information-sharing] => WP_Term Object ( [term_id] => 257 [name] => Information sharing [slug] => information-sharing-information-sharing [term_group] => 0 [term_taxonomy_id] => 257 [taxonomy] => issue [description] => What financial and project progress information must be shared between the parties? What is the required timeline for sharing information? How is the receiving party permitted to use the information received? Do the parties have the right to verify the information reported? [parent] => 49 [count] => 92 [filter] => raw [parent_name] => Protecting & sharing information [parent_slug] => information-sharing ) [insurance] => WP_Term Object ( [term_id] => 109 [name] => Insurance [slug] => insurance [term_group] => 0 [term_taxonomy_id] => 109 [taxonomy] => issue [description] => [parent] => 50 [count] => 62 [filter] => raw [parent_name] => Liability [parent_slug] => liability ) [ip-ownership] => WP_Term Object ( [term_id] => 48 [name] => Intellectual property [slug] => ip-ownership [term_group] => 0 [term_taxonomy_id] => 48 [taxonomy] => issue [description] => [parent] => 0 [count] => 0 [filter] => raw [parent_name] => [parent_slug] => ) [liability] => WP_Term Object ( [term_id] => 50 [name] => Liability [slug] => liability [term_group] => 0 [term_taxonomy_id] => 50 [taxonomy] => issue [description] => [parent] => 0 [count] => 0 [filter] => raw [parent_name] => [parent_slug] => ) [license-grants] => WP_Term Object ( [term_id] => 88 [name] => License grants [slug] => license-grants [term_group] => 0 [term_taxonomy_id] => 88 [taxonomy] => issue [description] => Are any licenses granted for the use of background or foreground intellectual property? What is the scope of the licensed intellectual property? What is the territory of the license? Is the license exclusive or non-exclusive? Are there any restrictions on the use of the licensed intellectual property? Are there any specific obligations to exploit the licensed intellectual property? Can the licensee grant sublicenses to third parties? Will products manufactured under license be marketed as branded or generic? (i.e. will they bear the licensor’s trademarks/trade dress) [parent] => 48 [count] => 96 [filter] => raw [parent_name] => Intellectual property [parent_slug] => ip-ownership ) [ownership-ip] => WP_Term Object ( [term_id] => 87 [name] => Ownership of IP [slug] => ownership-ip [term_group] => 0 [term_taxonomy_id] => 87 [taxonomy] => issue [description] => [parent] => 48 [count] => 71 [filter] => raw [parent_name] => Intellectual property [parent_slug] => ip-ownership ) [royalties-and-payments] => WP_Term Object ( [term_id] => 70 [name] => Payment structures [slug] => royalties-and-payments [term_group] => 0 [term_taxonomy_id] => 70 [taxonomy] => issue [description] => What is the payment structure under this agreement? What are the mechanisms to limit exposure to additional payments or expenses? [parent] => 53 [count] => 79 [filter] => raw [parent_name] => Business model [parent_slug] => business-model ) [outbreak-preparedness] => WP_Term Object ( [term_id] => 102 [name] => Preparedness & response [slug] => outbreak-preparedness [term_group] => 0 [term_taxonomy_id] => 102 [taxonomy] => issue [description] => [parent] => 46 [count] => 13 [filter] => raw [parent_name] => Equitable access [parent_slug] => access-to-medicines ) [supply-purchase-of-products] => WP_Term Object ( [term_id] => 268 [name] => Product supply [slug] => supply-purchase-of-products [term_group] => 0 [term_taxonomy_id] => 268 [taxonomy] => issue [description] => [parent] => 53 [count] => 43 [filter] => raw [parent_name] => Business model [parent_slug] => business-model ) [information-sharing] => WP_Term Object ( [term_id] => 49 [name] => Protecting & sharing information [slug] => information-sharing [term_group] => 0 [term_taxonomy_id] => 49 [taxonomy] => issue [description] => [parent] => 0 [count] => 0 [filter] => raw [parent_name] => [parent_slug] => ) [protection-results] => WP_Term Object ( [term_id] => 90 [name] => Protection of IP [slug] => protection-results [term_group] => 0 [term_taxonomy_id] => 90 [taxonomy] => issue [description] => [parent] => 48 [count] => 70 [filter] => raw [parent_name] => Intellectual property [parent_slug] => ip-ownership ) [publication-of-results] => WP_Term Object ( [term_id] => 290 [name] => Publication of results [slug] => publication-of-results [term_group] => 0 [term_taxonomy_id] => 290 [taxonomy] => issue [description] => What information are the parties required or permitted to publish? What is the required timeline for making data available? What are the acceptable publication channels? Is compliance with a specific open access policy required? [parent] => 49 [count] => 61 [filter] => raw [parent_name] => Protecting & sharing information [parent_slug] => information-sharing ) [quality-management] => WP_Term Object ( [term_id] => 372 [name] => Quality management [slug] => quality-management [term_group] => 0 [term_taxonomy_id] => 372 [taxonomy] => issue [description] => [parent] => 53 [count] => 36 [filter] => raw [parent_name] => Business model [parent_slug] => business-model ) [regulatory-strategy] => WP_Term Object ( [term_id] => 56 [name] => Regulatory strategy [slug] => regulatory-strategy [term_group] => 0 [term_taxonomy_id] => 56 [taxonomy] => issue [description] => [parent] => 53 [count] => 53 [filter] => raw [parent_name] => Business model [parent_slug] => business-model ) [warranties] => WP_Term Object ( [term_id] => 81 [name] => Representations & warranties [slug] => warranties [term_group] => 0 [term_taxonomy_id] => 81 [taxonomy] => issue [description] => Should the parties make any warranties, and if so, what is the scope? [parent] => 50 [count] => 88 [filter] => raw [parent_name] => Liability [parent_slug] => liability ) [technology-transfer] => WP_Term Object ( [term_id] => 86 [name] => Technology transfer [slug] => technology-transfer [term_group] => 0 [term_taxonomy_id] => 86 [taxonomy] => issue [description] => What is included in the technology and/or materials to be transferred? What are the responsibilities of each party to in relation to the transfer of materials and/or technology? [parent] => 49 [count] => 41 [filter] => raw [parent_name] => Protecting & sharing information [parent_slug] => information-sharing ) [term-and-termination] => WP_Term Object ( [term_id] => 52 [name] => Term & termination [slug] => term-and-termination [term_group] => 0 [term_taxonomy_id] => 52 [taxonomy] => issue [description] => Term What is the term of the agreement? Is it tied to the timeline of the project or license grants? Termination Under what circumstances may a party terminate or withdraw from the agreement? Effects of Termination What are the effects of termination or withdrawal by a party? [parent] => 0 [count] => 0 [filter] => raw [parent_name] => [parent_slug] => ) [term-of-agreement] => WP_Term Object ( [term_id] => 76 [name] => Term of agreement [slug] => term-of-agreement [term_group] => 0 [term_taxonomy_id] => 76 [taxonomy] => issue [description] => [parent] => 52 [count] => 87 [filter] => raw [parent_name] => Term & termination [parent_slug] => term-and-termination ) [termination-and-withdrawal] => WP_Term Object ( [term_id] => 74 [name] => Termination & withdrawal [slug] => termination-and-withdrawal [term_group] => 0 [term_taxonomy_id] => 74 [taxonomy] => issue [description] => [parent] => 52 [count] => 91 [filter] => raw [parent_name] => Term & termination [parent_slug] => term-and-termination ) [territory-access-commitments] => WP_Term Object ( [term_id] => 282 [name] => Territory access commitments [slug] => territory-access-commitments [term_group] => 0 [term_taxonomy_id] => 282 [taxonomy] => issue [description] => How should ‘territory’ be defined under the agreement? Should the definition make a distinction between different types of purchaser (e.g. public sector vs. private sector)? Should the developer be required to apply for regulatory approval in priority access markets? Should the developer be required to commit a proportion of the product manufactured to a certain country or purchasing organization? Should the developer be required to identify a third party that could fulfill supply requirements for the access territories in the event that the developer does not? Should the agreement include any anti-diversion provisions? [parent] => 46 [count] => 58 [filter] => raw [parent_name] => Equitable access [parent_slug] => access-to-medicines ) ) [filter_issues:GHIAA2019\MapguideSearch:private] => Array ( ) )