Articles
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May 16, 2024 |
outsourcedpharma.com | Louis Garguilo |Mark Witcher |Mel Palmer |Victoria Meyer
Emerging biotherapies are enabling transition from traditional intravenous therapies to subcutaneous administration. The formulation of some biotherapies may present delivery challenges, such as larger volumes and viscosities that require innovative, patient-friendly delivery system design.
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May 9, 2024 |
biosimilardevelopment.com | Matthew Pillar |Alex Santos |Geoff Middleton |Victoria Meyer
Get more biosimilar development insight with our FREE newsletter Newsletter | May 9, 2024 Webinar: Key Elements of Process and Analytical Development to Support Biologics Tech TransferJoin us on May 13th as our expert panel discusses the intricacies of technology transfer, drawing from real-life case studies. Investigate critical components for success, risk assessment, and effective mitigation strategies.
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Apr 25, 2024 |
biosimilardevelopment.com | K. Coleman |Erich Bozenhardt |Victoria Meyer |P. Bhendale
Get more biosimilar development insight with our FREE newsletter Newsletter | April 25, 2024 Webinar: Key Elements of Process and Analytical Development to Support Biologics Tech TransferJoin us on May 13th as our expert panel discusses the intricacies of technology transfer, drawing from real-life case studies. Investigate critical components for success, risk assessment, and effective mitigation strategies.
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Sep 21, 2023 |
biosimilardevelopment.com | Fran DeGrazio |Aditi Shivarkar |Victoria Meyer
Get more biosimilar development insight with our FREE newsletter Newsletter | September 21, 2023 The FDA now defines a prefilled syringe, a product that was at one point considered “packaging” for a drug, as a constituent part of a combination product.
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May 25, 2023 |
pharmaceuticalonline.com | Victoria Meyer |Joe Hoff |Oliver Stauffer |Grant Merrill
A conversation with Vanessa Figueroa, Rebecca Brewer, and Greg Gibb, Quality Executive Partners In the first of this two-part series, microbiology and contamination control specialists Vanessa Figueroa, Rebecca Brewer, and Greg Gibb, Ph.D., discuss best practices in developing contamination control strategies through the lens of the newly formalized provisions in the EU GMP Annex I, .
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