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| Winning Strategies For Commercial Manufacturing Leaders | E-Book | Pii, A Jabil Company | Complex formulations, HPAPIs, and modified-release products demand early planning. Formulation strategy, tech transfer, infrastructure, and partner selection largely determine scale-up success. |
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| Powder Rheology: Gateway For Tablet Sticking Insights | Application Note | By Devang Patel, Kerry Cruz, et al., Natoli Engineering Company, Inc. | Powder rheology offers a scientific method to predict and mitigate tablet sticking issues, helping to ensure smoother pharmaceutical production cycles through early material and tooling selection. |
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By Louis Garguilo, Chief Editor, Outsourced Pharma | A CDMO employs accomplished professionals, operates modern facilities, and still frustrates the heck out of you. Accumulated talent and capabilities are impressive, but closer examination reveals the problem lies between the lines of the CDMO’s work demarcations. Instead, you need your CDMO to operate as a constellation of unified skills. Chief Editor Louis Garguilo explores this "holistic pattern of work that forms an interconnected organization, and presents a clear picture of management and culture." | |
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Expanding Global Access Through Voluntary Licensing And Tech Transfer | A conversation with Charles Gore, Medicines Patent Pool | Turning patented biomedical discoveries into affordable, widely available treatments requires aligned partnerships between innovator pharma and regional generic manufacturers. In this episode of Outsourcing Against the Outbreak, Charles Gore, Executive Director of the Medicines Patent Pool (MPP), breaks down how voluntary licensing models expand access across low- and middle-income markets. |
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INDUSTRY INSIGHTS CONTINUED |
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| The Art of Formulation | Infographic | Altasciences | Explore how Altasciences integrates pharmaceutical formulation development with nonclinical research to optimize drug formulations, assess risks, and support progression to FIH trials. |
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| De-Risking Complex Generic OSD Development | Case Study | Recipharm | Complex generic tablet development requires early alignment of regulatory strategy, QbD formulation, discriminatory dissolution, and reference-scaled bioequivalence. |
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| Seamless Commercial Tech Transfers In OSD Manufacturing | Article | By Rebecca Peek and Laura Treche, Lonza | A structured approach to OSD tech transfer, from NPI through PPQ and CPV, can compress timelines significantly, as one case study illustrates with full PPQ completion in under six months. |
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| Continuous Manufacturing For API Breakthroughs | White Paper | By Dr. Satyanarayana Tummanapalli and Dr. Muralikrishna Valluri, Curia | Observe how a compound library, designed for chemical diversity and lead-like properties, uses advanced filtering to improve hit discovery, speed hit-to-lead development, and boost drug discovery. |
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| From Powder To Particles With Jet Milling | Webinar | Lonza | Gain valuable insights into the jet milling process and Quality by Design approach for inhalation drug delivery and their potential applications in drug development. |
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OUTSOURCED PHARMA CAPABILITIES UPDATE |
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CDMOs in biologics, cell and gene, and small molecule share their capabilities and available capabilities. See for yourself why this virtual event has become a wildly popular resource to identify options for your development and manufacturing needs. |
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| Connect With Outsourced Pharma: |
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