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International Side Effects Week: How you can (sometimes) prevent side effects yourself

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Starodub Whitepapers

Approaches to include drug substance quality information in a drug product application (June 2022)

Published on June 2022

How to select a cell line to produce a biosimilar (June 2021)

Published on June 2021

Combination products in the EU MDR (May 2021)

Published on May 2021

News on the Postponement of the EU Medical Device Regulation, Corrigenda and MDCG guidance (June 2020)

Published on June 2020

EU MDR impact on importers and distributors (March 2020)

Published on March 2020

Biopharmaceutical products – Do you have your reference standard program in place? (December 2019)

Published on December 2019

Radiopharmaceuticals – How to Register in EU? (October 2019)

Published on October 2019

Is your Active Pharmaceutical Ingredient quality control strategy up to standard? (July 2019)

Published on July 2019

What is new under the EU MDR for software manufacturers? (December 2018)

Published on December 2018

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