Medivdpharma (MIP) – Keeping Your QMS Audit-Ready, Always
At Medivdpharma (MIP), we make quality management simple and reliable for medical device and life sciences companies. Whether you’re running a paper-based system or moving to an eQMS, we ensure your QMS works for you — not against you.
With decades of experience in quality assurance and regulatory affairs, our team goes beyond box-ticking. We help you build a QMS that:
- Implementation of QMS Services for Startup Companies
- Manage your QMS System
- Meets ISO13485, MDR, IVDR, UKMDR, FDA 21 CFR Part 820, ISO15189 and MDSAP requirements
- Stays audit-ready for regulators, Notified Bodies, and unannounced inspections
We close compliance gaps before they become problems — giving you peace of mind, confidence in every audit, and the freedom to focus on growth instead of red tape.
