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Publication
2025
Driving an Innovative Biologics Pipeline in India
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Publication
2025
IPA USTR 2024 Special 301 Submission
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Publication
2025
Best Practices for Authentication Track Trace in Pharmaceutical Products Packaging
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Publication
2025
Nitrosamines Drug Substance Related Impurities (NDSRIs)
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Publication
2025
Bain & Co: Healing the World - A Roadmap for Making India a Global Pharma Exports Hub
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Publication
2024
Changing Dynamics of Indian Pharma Supply Chain
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Publication
2024
IPA USTR 2023 Special 301 Submission
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Publication
2024
Guidance on Process Analytical Tools (PAT) in Oral Solids and API
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Publication
2024
Guidance on Good Engineering Practices
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Publication
2024
Deepening The Responsible Business Agenda
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Publication
2023
G20 Side Event – Indian Pharmaceutical Industry: Overview & Way Forward
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Publication
2023
Best Practices on Digital Data Management 21 CFR Part 11 Compliance
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Publication
2023
Human Error Reduction
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Publication
2023
Guidance for Technology Transfer
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Publication
2023
Market Access Barriers in the Pharmaceutical Sector in India’s Key Export Destinations
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Publication
2023
Guidance on Nitrosamine Impurities
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Publication
2023
IPA USTR 2022 Special 301 Submission
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Publication
2022
Global Innovation Summit 2021 – Action Report
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Publication
2022
Funding Innovation & R&D in Indian Pharma
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Publication
2022
Innovation Index & Ecosystem Framework
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Publication
2022
5 Key Imperatives to Build India’s Innovation Ecosystem
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Publication
2022
IPA USTR 2021 Special 301 Submission
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Publication
2021
Focus on API Manufacturing to Reduce Import Dependency
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Publication
2021
Best Practices in Media Fill for Sterile Products
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Publication
2021
Opportunities for Achieving Vision 2030
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Publication
2021
Expanding India’s Global Regulatory Footprint
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Publication
2021
Cleaning Methodology & Validation
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Publication
2021
Assessment of India’s Current Innovation Ecosystem
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Publication
2021
Pharma Innovation Index – India
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Publication
2021
IPA Submission to RCGM – Regulatory Perspective on Biosimilars
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Publication
2021
IGBA Vision Report
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Publication
2021
Opportunities For Achieving Vision 2030
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Publication
2021
6 Growth Tailwinds for Generics & Biosimilars
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Publication
2021
Vaccination: Myths vs Facts
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Publication
2021
Indian Pharma’s Role in Public Health & Economic Growth
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Publication
2021
Vision 2030: Growth Aspiration for Indian Pharma
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Publication
2021
Visual Inspection in Sterile Manufacturing
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Publication
2021
Regulatory Best Practices – First Cycle ANDA Approvals
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Publication
2021
Regulatory Best Practices – Focus on Post Approval Changes and Change Control Evaluation
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Publication
2021
IPA USTR Special 301 Submission
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Publication
2021
IPA Employee Safety Initiatives Report
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Publication
2020
Catalyzing Pharma-MedTech Innovation – Committee Paper
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Publication
2020
Accenture: Reviving Ancillary Pharma Industry – Resilience Roadmap
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Publication
2020
IPA x BCG: Future of Work – Quality Function
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Publication
2020
Reviving India’s API Industry
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Publication
2020
Future of Work – New Commercial Operating Model
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Publication
2020
Appendix 1 – Regulatory Subgroup Annexure 2A
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Publication
2020
IPA x Samhita: CSR Report - Beyond Business
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Publication
2020
Safety Protocols During COVID for Plant Personnel
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Publication
2020
IIMA Case Study – COVID Response
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Publication
2020
COVID-19: Best Practices in Employee Safety
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Publication
2020
Market Complaints: Handling Best Practices
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Publication
2020
Product Robustness & Lifecycle Management
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Publication
2020
Analytical Method Development: Chromatography & Particle Size
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Publication
2020
USTR Special 301 Submission – 2020
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Publication
2019
Indian Pharma & the Global Market
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Publication
2019
Strengthening India’s Innovation Ecosystem – Discover in India
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Publication
2019
Indian Pharmaceutical Industry – The Way Forward
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Publication
2019
USTR Special 301 Submission – 2019
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Publication
2019
Global Healthcare Policy Trends: India’s Perspective (Warsaw)
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Publication
2019
Batch Failure Investigations – Focus on Non-Conformities
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Publication
2019
Pharma Sector Overview – Presentation (Mumbai)
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Publication
2018
Good Documentation Practices in Pharma
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Publication
2018
Process Validation in Pharmaceutical Manufacturing
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Publication
2018
USTR Special 301 Submission – 2018
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Publication
2018
Patent Working: IPA Comments – March 2018
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Publication
2017
USTR Special 301 Submission – 2017
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Publication
Promoting API Manufacturing – Invest India 2017
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Publication
2017
Unlocking Pharma Growth – Emerging Markets (Medicines for Europe)
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Publication
2017
India’s Affordable Healthcare Contribution – AAPI Convention
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Publication
2017
Data Reliability in Pharmaceutical Systems
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Publication
2016
Licensing of Generic Products: Industry Expectations – IGDRP Presentation, Strasbourg
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Publication
2016
USTR: 2016 Special 301 Submission – 5 Feb 2016 (Docket No. USTR–2015–0022)
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Publication
2016
IPA-FDA Quality Forum Update – Washington DC, June 2016
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Publication
2015
TRIPS Article 39.3 & Data Exclusivity – Presentation to Health Secretary
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Publication
2015
Comments on India’s National IPR Policy
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Publication
2015
IPA-FDA Collaborative Meeting – Washington DC
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Publication
2015
IPA-FDA Quality Forum – Washington DC
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Publication
2015
Pharma Policy Presentation – Carnegie Endowment, Washington DC
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Publication
2014
USTR OCR: Special 301 Review – 2014
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Publication
2014
USITC Written Submission – Investigation No. 332-543
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Publication
2014
USTR Special 301 Review – Response to Testimony (2014)
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Publication
2014
CII 12th National Pharma Conclave – Industry Perspective
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Publication
2014
IPA-FDA Workshop on Quality Systems – Feedback Report (Mumbai, 2014)
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Publication
2014
USITC Pre-Hearing Statement – Investigation No. 332-543
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Publication
2014
Access to Medicines & UHC – IPA Innovation Dialogue, Chennai
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Publication
2014
National Conference on Pharma Policy & DPCO 2013 – New Delhi
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Publication
2013
GoM Impact Assessment – NPPP 2012, New Delhi
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Publication
2013
Role & Contribution of India’s Pharma Industry
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Publication
2012
Backgrounder on Intellectual Property Rights
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Publication
2012
IP Protection Symposium – NPPP 2011, Jodhpur
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Publication
2012
GoM NPPP 2011: Calibrated Policy Roadmap – New Delhi
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Publication
2012
Roundtable with US HHS Secretary – Mumbai
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Publication
2011
BioSpectrum Forum 2011 – Road to Success for Indian Pharma
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Publication
2011
Comments on Utility Model Discussion Paper
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Publication
2011
SCM Pharma India 2011 – Anti-Counterfeit Measures, Mumbai
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Publication
2011
Comments on IPO Organizational Structure Discussion Paper
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Publication
2010
Comments on India’s IPR Regime Discussion Paper
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Publication
2010
Comments on Compulsory Licensing Discussion Paper
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Publication
2010
Data Protection vs Data Exclusivity – IPA Viewpoint
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