Insights On Pharmaceutical Logistics

31. Shedding Light On Photo-Stability Forced Degradation 11/26/2024

    Ensure the stability and safety of your drug products by utilizing comprehensive forced degradation and photo-stability testing, guided by ICH and FDA standards, to identify degradation pathways and assess light exposure risks.

32. Building A Purification Toolkit For An Expanding Variety Of mAb Therapeutics 5/29/2025

    Explore techniques for optimizing purification toolkits for various monoclonal antibody formats. This session covers resin and buffer selection for efficient downstream process development.

33. Implementing A Disaster Recovery Plan 8/23/2024

    When facing a malfunction, having an effective disaster recovery plan can make the difference between a swift fix, and losing your samples and time.

34. Pharmaceutical Supply Chain Management Best Practices 9/13/2024

    Explore strategies for effective supply chain management and overcoming modern supply chain challenges in the pharmaceutical industry.

35. A Temperature-Stable Replacement For Animal Trypsin In Cell Dissociation Applications 6/9/2025

    Improve cell dissociation with a gentle, recombinant enzyme. This temperature-stable protease shows dissociation kinetics similar to porcine trypsin but with lower cell toxicity and greater overall purity.

36. Quality Roundtable: Raw Material Planning For Tech Transfer And Scaling Biologics 1/22/2025

    Join this roundtable of biopharmaceutical professionals as they share their insights to help you navigate important quality and planning decisions for the progression of your biologic.

37. Outsourcing To ISO 17025 Accredited Suppliers 1/28/2025

    Discover the advantages of outsourcing equipment calibration to ISO 17025 accredited suppliers, including cost efficiency and regulatory assurance, in our detailed analysis. Read more to transform your calibration processes.

38. Top Safety Considerations In Biopharmaceutical Manufacturing 4/16/2025

    Understanding top safety concerns, from combustible material handling and chemical exposure to HPAPIs, is the first step toward preventing accidents in biopharmaceutical manufacturing environments.

39. Scaling For Success: Preparing Your Cell Culture Workflow 7/21/2025

    Uncover how early planning of medium, feed systems, and manufacturing workflow can mitigate costs, reduce delays, and accelerate therapeutic delivery to patients.

40. Moving Batch Release Into The Fast Lane 1/21/2026

    Complex supply chains and fragmented systems slow batch release, delaying patient access and revenue goals. Learn how automation and centralized data improve compliance and accelerate delivery.