Showing 49–60 of 70 results
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Pharmaceutical Dissolution Testing: Practical Training
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Implementing ISO 13485:2016 and MDSAP
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Upstream Process Development for Biopharmaceuticals
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Medical Devices: Brexit and the UK Responsible Person
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An Introduction to Biopharmaceuticals: A Beginner’s Guide
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Clinical Trial Optimisation for Excellent Delivery
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Understanding Medical Device Software Requirements in the EU and US
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Interpreting and Applying ISO 14971 Risk Management
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Root Cause Analysis in Life Sciences
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Understanding Aseptic GMP for Cell and Gene Therapies
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Stability Testing and Evaluation (ICH Q1E) for Pharmaceuticals
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Technical Writing for Pharmaceutical Professionals
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