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

Thursday, October 10th

News

Update of the list of harmonized standards under Regulations (EU) 2017/745 (MDR) and (EU) 2017/76 (IVDR)

The Commission Implementing Decisions (EU) 2024/2631 and (EU) 2024/2625 have been published in the Official Journal of the European Union on October 9, 2024. These amend the list of harmonized standards under MDR and IVDR, respectively.

DOWNLOAD IMPLEMENTING DECISION 2024/2631

DOWNLOAD IMPLEMENTING DECISION 2024/2625

Update of the list of harmonized standards under Regulations (EU) 2017/745 (MDR) and (EU) 2017/76 (IVDR)

Content

share

Related Posts

Events