Services
- CertificationWhatever the size of your company, wherever you are based, and whatever the category of your medical devices, we make it our mission to support you throughout your certification process.
- TrainingThe GMED North America Training Center delivers to you its expertise to enhance and develop your skills.
  - Training Catalog
  - Request a Training
- Focus on Medical DevicesTechnical and regulatory information in key medical device fields.
Company
- CompanyGMED’s level of excellence and standards have made it an internationally recognized name in the field of medical device certification.
Knowledge Center
Events

Certification Application

Wednesday, March 13th

News

Update of the list of harmonised standards under Regulations (EU) 2017/745 (MDR) and (EU) 2017/746 (IVDR)

The Commission Implementing Decisions (EU) 2024/815 and (EU) 2024/817 have been published in the Official Journal of the European Union on March 8, 2024. These amend the list of harmonized standards under the MDR and IVDR, respectively.

DOWNLOAD IMPLEMENTING DECISION 2024/815

DOWNLOAD IMPLEMENTING DECISION 2024/817

Update of the list of harmonised standards under Regulations (EU) 2017/745 (MDR) and (EU) 2017/746 (IVDR)

Content

share

Related Posts

Events