MDSAP Compliance and Audit Success
The webinar was successfully concluded on
March 07, 2024
In a nutshell, during the webinar, our presenters – Pawan Sadhnani and Anuradha Gore discussed the following topics:
- Introduction and Overview of MDSAP.
- Country-specific Compliance Requirements: Best Practices and Tips.
- Anecdotes from the Audit World: Engaging Stories and Real-life Examples that Shed Light on Auditing.
- Challenges During Compliance & Audits.
- MDSAP Benefits.
As a continuous practice, Freyr organizes more webinar sessions related to Regulatory aspects in Life Sciences. We presume you would like to be a part of all those sessions. If yes, let us have an opportunity to inform you about our next session.
Pawan is an accomplished Strategy Consultant specializing in the Medical Device, SaMD, and IVD domains. His commitment is to deliver comprehensive end-to-end Regulatory solutions, guiding organizations through complex compliance landscapes for successful market access and global expansion. He excels in crafting tailored Regulatory strategies that cater to the unique needs of healthcare industry stakeholders, adeptly navigating organizations through intricate compliance requirements for seamless transitions and strategic implementations.
Anuradha Gore, a seasoned Senior Manager at Freyr, brings over eighteen (18) years of experience in the Biotechnology and Medical Device industry. Serving as a QMS Subject Matter Expert and a Certified Lead Auditor for ISO 13485, ISO 9001, and MDSAP, Anuradha has extensive experience in planning strategies and implementing ISO 13485, ISO 9001, 21 CFR 820, and MDSAP across a diverse portfolio of medical devices, IVDs, and SaMD.
Hosted By
Pawan Sadhnani
Strategy Consultant, MDV
Presented By
Anuradha Gore
Senior Manager MDV, QMS Team