Medical Devices / In Vitro Diagnostics
Let the AMS Medical Device Expert group
help you generate solutions:
Get premarket or postmarket phase aid for:
- Classification
- Regulatory tasks
- Planning and conduct of clinical investigations / clinical performance studies around your product
- Medical Device Vigilance
Talk or write to us: Research@ams-europe.com
AMS also supports you in preparing HTA documents for benefit assessments of medical devices.
