Qmed Consulting A/S
Clinical development services, clinical trial management and regulatory affairs.
What they do
From their website
/services/regulatory-affairs
/services/regulatory-affairs/iso-13485-consulting
/services
- Post-market surveillance (opens in a new tab)
- Data management and analytics (opens in a new tab)
- Clinical evidence generation (opens in a new tab)
- MDR / IVDR classification (opens in a new tab)
- Market access (opens in a new tab)
- PMCF execution (opens in a new tab)
- Udi & eudamed (opens in a new tab)
- Quality and compliance support (opens in a new tab)