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International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH)
ICH Q9 – Quality Risk Management
25 mins
Intermediate
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Risk management in the life sciences is a proactive process designed to identify, assess, and mitigate potential risk that could impact regulatory compliance and patient safety. This involves a systematic approach to understanding and addressing risks associated with drug development, clinical trials, manufacturing, distribution, and post-market surveillance.
International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH)
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