Services
- Services
- Regulatory affairs
Regulatory affairs
Meddoc provides all tasks related to clinical trials and marketing authorization
Full description
We manage marketing authorization for pharmaceuticals
Our services include:
All tasks related to submission of application in Denmark for marketing authorization Submission of variations Submission of safety reports
We manage CE-marking of medical devices
Our services include:
All tasks related to application for CE-marking All tasks related to clinical trials
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Service contact
Company details
Remedium
Remedium is the Northern European Contract Research Organisation able to deliver to you a qualified Clinical Research framework for conducting your clinical trials
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