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Quality Risk Management (QRM) in Pharmaceutical Industry
2022-01-06
Quality Risk Management (QRM) is the process of identifying, evaluating, and mitigating recognized risks connected with medicines and healthcare goods. An excellent Quality Risk Management programme can be created to reduce risk to a manageable level and deliver high-quality products to protect citizens' health.
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Training Program for CMC Leaders - EU edition
24th March - 05th December, 2025
Rich with practical insights and real-world applications
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Process Validation for Biotechnological Products MasterClass - EU edition
07-10 April, 2025
Today, process validation comprises three main steps:
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Process Validation for Biotechnological Products MasterClass - US edition
07-10 April, 2025
Understand how to qualify scale-down models
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