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Medical Device Regulation in Europe
2022-08-16
Medical device efficacy and safety have always been of utmost significance in Europe.
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Entry Level Process Validation for Biotechnological Products MasterClass - EU edition
18-21 November, 2024
QbD concept, process validation, and regulatory requirements!
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CRO Oversight MasterClass - EU edition
18-21 November, 2024
How to design and implement the systems your company needs.
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CRO Oversight MasterClass - US edition
18-21 November, 2024
The latest revision to ICH GCP
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