- Bone Health
- Immunology
- Hematology
- Respiratory
- Dermatology
- Diabetes
- Gastroenterology
- Neurology
- Oncology
- Ophthalmology
- Rare Disease
- Rheumatology
Tahir Amin: Transparency in Drug Pricing
Tahir Amin, DipLP, co-founder and director of intellectual property of Initiative for Medicines, Access, and Knowledge, a public interest team of attorneys and scientists who ensure that patents do not obstruct access to affordable medicines for patients in the United States and around the world, discusses transparency in drug pricing.
Transcript:
Drug makers often argue that developing a drug is so costly that high prices are warranted to recoup their costs and reward innovation. What do you think about that argument?
I think that’s a fair argument, and we know that there are a lot of costs that go into drug development and research. What those exact costs are we don’t exactly know, it’s a bit of a black box, and I think some transparency around that would be helpful so that these debates and these discussions can be more informed. But we don’t believe that all the various patents that are being filed warrant or explain all the costs and the sort of profits that are being made as a result of these strategies that companies are using in order to prevent competition.
I think those are separate issues, and they need to be unpackaged better to have a better policy to help both the payers and the public in order to get fairer pricing; but also to actually better improve what kind of [research and development, R&D] is done, what kind of innovation comes out of the system because at the moment I feel the patent system is an incentive mechanism which is not functioning at its highest possible way.
Boosting Health Care Sustainability: The Role of Biosimilars in Latin America
November 21st 2024Biosimilars could improve access to biologic treatments and health care sustainability in Latin America, but their adoption is hindered by misconceptions, regulatory gaps, and weak pharmacovigilance, requiring targeted education and stronger regulations.
Biosimilars Policy Roundup for September 2024—Podcast Edition
October 6th 2024On this episode of Not So Different, we discuss the FDA's approval of a new biosimilar for treating retinal conditions, which took place in September 2024 alongside other major industry developments, including ongoing legal disputes and broader trends in market dynamics and regulatory challenges.
Breaking Down Biosimilar Barriers: Interchangeability
November 14th 2024Part 3 of this series for Global Biosimilars Week, penned by Dracey Poore, director of biosimilars at Cardinal Health, explores the critical topic of interchangeability, examining its role in shaping biosimilar adoption and the broader implications for accessibility.
Breaking Down Biosimilar Barriers: Payer and PBM Policies
November 13th 2024Part 2 of this series for Global Biosimilars Week dives into the complexities of payer and pharmacy benefit manager (PBM) policies, how they impact biosimilar accessibility, and how addressing these issues may look under a second Trump term.
