Biopharmaceutical Alliance Launched by India, South Korea, US, Japan, and EU
- Oct 2, 2023
- 5 min
Key Players in Medical Device Regulation: Economic Operators under EU MDR and IVDR
- Sep 30, 2023
- 3 min
Class I Medical Devices and CE Marking: Compliance Essentials
- Sep 29, 2023
- 5 min
Navigating the Complex World of Combination Products: Understanding EU MDR Article 117
- Sep 28, 2023
- 4 min
Certifying Medical Devices in the EU: The Crucial Role of Notified Bodies under MDR and IVDR
- Sep 27, 2023
- 4 min
The CE Mark is Just the Beginning: Post-CE Compliance under EU MDR
- Sep 24, 2023
- 6 min
Deciphering Medical Device Risk Classification Under EU MDR
- Sep 23, 2023
- 5 min
Navigating the EU MDR Labelling Requirements: A Comprehensive Guide
- Sep 21, 2023
- 7 min
Understanding System and Procedure Packs in Accordance with EU MDR
- Sep 18, 2023
- 4 min
Understanding the CE Marking Process for Medical Devices in the EU
- Sep 17, 2023
- 8 min
Regulation of Reprocessed Single-Use Devices (SUD) under EU MDR
- Sep 16, 2023
- 5 min
Reprocessing Single-Use Devices in accordance with EU Medical Device Regulations (EU MDR 2017/745)
- Sep 15, 2023
- 4 min
Conformity Assessment of Medical Devices under EU MDR
- Sep 6, 2023
- 4 min
Meeting EU Regulations: The Role of the European Authorized Representative (EAR)
- Aug 28, 2023
- 5 min
Biologics and Biosimilar Regulations and Registration in the European Union (EU) (EMA)
Insights
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