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See allStatement at the fourth meeting of the open-ended Intergovernmental Working Group (IGWG 4) on the WHO Pandemic Agreement
On 1st December 2025 in Geneva, IFPMA delivered a statement at at the fourth meeting of the open-ended Intergovernmental Working Group (IGWG 4) on the WHO Pandemic Agreement.
Read moreWIPO Committee on IP and Development (CDIP 35): Technology Transfer
On 20 November 2025, IFPMA submitted a statement on technology transfer at the WIPO Committee on IP and Development (CDIP 35) in Geneva. Technology transfer in the pharmaceutical sector is a complex and resource-intensive process. It requires significant technical expertise, time, and investment, as well as a robust, stable, and predictable intellectual property framework, which...
Read moreBiopharmaceutical CEOs Roundtable met in Berlin
12 NOVEMBER 2025, Berlin – The Biopharmaceutical CEOs Roundtable (BCR), a global policy platform representing the world’s leading biopharmaceutical companies, convened last week in Berlin to discuss how pharmaceutical innovation can drive better health outcomes, strengthen economies, and enhance global health security. The BCR delegation also met with Federal Chancellor Merz, along with key members...
Read moreWIPO Standing Committee on Patents (SCP 37): Technology Transfer
On 5 November 2025, IFPMA delivered a statement on technology transfer at the WIPO Standing Committee on Patents (SCP 37) in Geneva. Technology transfer in the pharmaceutical sector is a complex and resource-intensive process. It requires significant technical expertise, time, and investment, as well as a robust, stable, and predictable intellectual property framework, which is...
Read moreWIPO Standing Committee on Patents (SCP 37): Patents and health
On 4 November 2025, IFPMA delivered a statement on patents and health at the WIPO Standing Committee on Patents (SCP 37) in Geneva. The International Federation of Pharmaceutical Manufacturers and Associations (IFPMA) represents the global research-based biopharmaceutical industry. We appreciate the opportunity to address the Committee on patents and health. Intellectual property is fundamental to...
Read moreStatement on PABS Instrument at the third meeting of the open-ended Intergovernmental Working Group (IGWG 3) on the WHO Pandemic Agreement
On 3 November 2025 in Geneva, IFPMA delivered a statement at at the tnird meeting of the open-ended Intergovernmental Working Group (IGWG 3) on the WHO Pandemic Agreement.
Read morePublications
See allConsiderations on the use of reliance in clinical trials review
The global clinical trial landscape is undergoing a profound transformation, driven by the increasing use of multiregional clinical trial designs, rapid advances in science and technology, and the growing need for coordinated regulatory approaches. With the expansion of multiregional clinical research, the need for harmonized regulatory frameworks has become more urgent. Despite this shift, regulatory...
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Policy considerations for the development, regulation and adoption of biosimilars
Biosimilars can play a role in expanding patient access to biological medicines and in supporting the sustainability of healthcare systems. To fully realize this potential, IFPMA recommends the adoption of a series of policy recommendations.
Read moreAdult immunization: A critical investment for health, equity, and economic resilience
Immunization is an effective public health strategy to help prevent and reduce the impact of infectious diseases throughout the life course. As populations age and non-communicable diseases (NCDs) increase, our societies are becoming more vulnerable to preventable infectious diseases. This can put a significant strain on health systems, societies, and economies. Vaccines are wide recognized...
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Expert insights
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Health as an economic priority – building on momentum driven by the G20 South Africa Presidency
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Getting procurement right: sustainable and secure supply chains that support access to medicines
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G7 Canada is an opportunity to unlock the potential of life sciences
Read moreResources
See allStreamlining samples management to strengthen health outcomes in Africa
Ensuring the quality, safety, and efficacy of pharmaceutical products is a cornerstone of public health. To meet these high standards, innovative multinational pharmaceutical companies perform rigorous batch release testing for every product, following internationally recognized protocols and approved specifications. However, countries may require additional in-country testing by their National Regulatory Authorities (NRAs) or National Control...
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Our Ethos in Action – Decision-Making Framework Toolkit
IFPMA has developed a Five-Phase Decision-Making Framework, grounded in the IFPMA Ethos or value system, to help companies make decisions that balance business objectives and ethical considerations to meet patient needs and the expectations of the medical community, regulators, and society.
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February 2024: Impact of a waiver of intellectual property rights for COVID-19 therapeutics
As discussions on an extension of a waiver of intellectual property (IP) rights on COVID-19 therapeutics continue, latest evidence and data published today explains what the adverse impact of a waiver may be on the entire innovation ecosystem and the consequences it may have on industry’s ability to fight future pandemics.
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