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International Side Effects Week: How you can (sometimes) prevent side effects yourself
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Comprehensive MDR Compliance: Key Recommendations for Medical Device Manufacturers
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Starodub Whitepapers
Approaches to include drug substance quality information in a drug product application (June 2022)
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June 2022
How to select a cell line to produce a biosimilar (June 2021)
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June 2021
Combination products in the EU MDR (May 2021)
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May 2021
News on the Postponement of the EU Medical Device Regulation, Corrigenda and MDCG guidance (June 2020)
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June 2020
EU MDR impact on importers and distributors (March 2020)
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March 2020
Biopharmaceutical products – Do you have your reference standard program in place? (December 2019)
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December 2019
Radiopharmaceuticals – How to Register in EU? (October 2019)
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October 2019
Is your Active Pharmaceutical Ingredient quality control strategy up to standard? (July 2019)
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July 2019
What is new under the EU MDR for software manufacturers? (December 2018)
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December 2018
Metehan Agaca
Senior RA Manager
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