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Updates
Change in distribution Direct Healthcare Professional Communication in the Netherlands
October 23, 2024
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Key Outcomes of LSH Dutch Mission to Japan: New Partnerships to Support Market Entry
October 16, 2024
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Article 61(10) of MDR: A Pathway for Medical Device Software?
October 15, 2024
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The Compliance Compass: Guiding Clinical Investigations for Medical Devices through ISO 14155 and MDR
October 11, 2024
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We Are Excited to Attend BioTechX 2024 in Basel!
October 4, 2024
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EMA Pilot Program for Orphan Medical Devices
October 3, 2024
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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)
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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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