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Biologics CDMO: Four Critical Aspects of Clinical Development, Manufacturing & Analysis

Are you ramping up for clinical development, and deciding which CDMO to outsource your biologic? Learn more about how to efficiently qualify a new biomanufacturing partner organization for their fit with your timelines, budgets, and regulatory needs. This webinar will cover new innovations that help mitigate risk, discuss how analytical support integration can speed timelines, and much more.

  • Learn four critical attributes you need to evaluate when outsourcing your clinical candidate with a biologics CDMO.
  • Gain insights on due diligence questions when selecting the right CDMO to accelerate your clinical candidate, for timing, capacity, technical expertise, international regulatory compliance, and collaboration.
  • Discover how to create an effective RFP for evaluating CDMO fit for your biologic program’s needs

Read More on Biopharm International