Newsletter Archive

31. 03.27.25 -- A Practical Guide To Defining Priority Data In MES 3/27/2025
    03/27/25 Pharmaceutical Online Newsletter
32. 03.27.25 -- STREAM Edition: Innovative Pathways In Biopharma: From Automated Drug Delivery To Eco-Design And Emerging CDMO Trends 3/27/2025

    03/27/25 Pharmaceutical Online Newsletter

33. 03.26.25 -- Revised EU GMP Annex 1: Your Compliance Guide 3/26/2025

    03/26/25 Pharmaceutical Online Newsletter

34. 03.26.25 -- Improving Bioprocess Efficiency With New Strategies And Innovations 3/26/2025

    03/26/25 Pharmaceutical Online Newsletter

35. 03.25.25 -- Fast-Track Your Path To Commercialization 3/25/2025

    03/25/25 Pharmaceutical Online Newsletter

36. 03.25.25 -- Generic Drug Approvals In Canada: Use Of A Foreign-Sourced Reference Product As A Canadian Reference Product 3/25/2025
    03/25/25 Pharmaceutical Online Newsletter
37. 03.22.25 -- Elevate OSD Manufacturing With Industry-Leading Technologies And Equipment 3/22/2025

    03/22/25 Pharmaceutical Online Newsletter

38. 03.21.25 -- Trends In FDA FY 2024 Inspection-Based Warning Letters 3/21/2025
    03/21/25 Pharmaceutical Online Newsletter
39. 03.20.25 -- Achieve Success In Upstream Bioprocessing: Prioritizing Productivity, Consistency, And Cost-Effectiveness 3/20/2025
    03/20/25 Pharmaceutical Online Newsletter
40. 03.20.25 -- Addressing Challenges In Automated Visual Inspection Of Lyophilized Vials 3/20/2025
    03/20/25 Pharmaceutical Online Newsletter