More and more medical device manufacturers are signing up for the Medical Device Single Audit Program (MDSAP) to accelerate market access and regulatory approval. The MDSAP model allows recognized Auditing Organizations to conduct a single audit that satisfies compliance requirements and regulatory requirements of participating authorities. This means that the MDSAP audit report can substitute routine agency inspections.
Watch this on-demand webinar with Srujesh Shah, Global Technical Program Manager with SAI Global, to learn:
- What is MDSAP?
- Should my organization certify to MDSAP?
- What does an MDSAP audit entail?
- What are the steps to obtaining MDSAP certification?