ICH Q12, Technical and Regulatory Considerations for Pharmaceutical Product Lifecycle Management, is a transformative document that will shape global regulatory submissions and practices. Adopted in November 2019, it has a wide scope of applicability across pharmaceutical drug substances and products (both chemical and biological), drug-device combination products that meet the definition of a pharmaceutical or biological product, as well as both new molecular entities and authorized products.
Hear about case studies relating to the application of Q12 principles
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Participate in an extended panel discussion with the invited experts via Q&A
Associate Director for Biosimilar & Regulatory Policy (Acting)
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