Enabling you to identify and mitigate the intrinsic risk in your operations, supply chains and business processes.
Evaluating how your products and services meet and exceed quality, safety, sustainability and performance standards.
Validating the specifications, value and safety of your raw materials, products and assets.
Biopharmaceutical stability studies are essential to assess sensitivity to factors that could cause aggregation and degradation which impacts biologic activity, product safety, and quality. But, what is important in the design and conduct of stability studies for biologic medicines? What are the potential “pit falls” and what steps can you take to ensure success? The challenges and real life case studies in biopharmaceutical stability studies are discussed during this short webinar with Intertek’s Biopharmaceutical Program Manager.
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