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Decontamination Process and the new Draft of the EU GMP Annex 1
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GMP Update series – What’s coockin’ – October 2020
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How to Qualify your suppliers in compliance with GMP
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Introduction à la réglementation sur les Dispositifs Médicaux
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New perspectives on Cross Contamination and Cleaning validation
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Remote audits – Why, when and how
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Starting materials – the GMP essentials
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Applying Control Charts for Visualizing and Detecting Trends
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EN ISO14971:2019 – Risk management – in relation to MDR and ISO13485
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Equipment Management in the Pharmaceutical Supply Chain
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IVDR Readiness – prepare for the changes in the new IVDR
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Maintaining Temperature Compliance for Pharmaceuticals in the Supply Chain
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MDR Audit Readiness
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