Featured Insights
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Biopharmaceutical Manufacturing Conference: Embracing Technology And Innovation
11/6/2024
Industry leaders gathered at the PDA Ireland Chapter event to discuss how innovation and technology are transforming biopharmaceutical manufacturing, addressing challenges, and driving efficiency.
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Best Practices In The Design Of A Pharmaceutical Manufacturing Facility
11/6/2024
A well-designed manufacturing facility is critical to ensuring product quality and regulatory compliance. Let's examine the importance of the concept design review in achieving these goals.
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How To Navigate The EU HTA Regulation For Better Market Access
10/21/2024
The EU's new Health Technology Assessment Regulation poses challenges and opportunities for the biopharma industry, making manufacturers adapt to unpredictable PICOs and prioritize scenario planning.
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Empowering Healthcare Decision-Making
10/21/2024
FormularyDecisions, now part of Cencora, has evolved significantly since its acquisition in 2019. Let's reflect on its journey, impact, and the future of formulary submissions in the digital age.
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The Unintended Consequences Of The Inflation Reduction Act (IRA)
10/21/2024
Cencora PayerPulse provides insights into market access trends and the Inflation Reduction Act's impact on Medicare Part D, based on research from 41 advisors.
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Industry Insights In Isolator Technologies And Aseptic Processing In Pharma
8/30/2024
Explore an overview of trends and insights in isolator technologies and aseptic processing in the pharmaceutical industry.
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What The Shift To The EMA's PMS Means For Industry
8/30/2024
Explore the implications of the shift to the European Medicines Agency's Pharmacovigilance System Master File (PMS) database for the pharmaceutical industry.
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Balancing Customization And Standardization With Targeted Medicines
8/30/2024
Examine an overview of the challenges companies face in handling regulatory differences when manufacturing targeted medicines.
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ICH Q2 And ICH Q14 Revisions Clarify Analytical Methods For Biologics
8/30/2024
Learn about the revisions to ICH Q2 and Q14 that provide clarification on analytical methods for biologics, aiming to ensure accuracy, reliability, and consistency in testing these products.