Aligning supplier evaluation practices with US FDA and ISO 13485 requirements
The webinar was successfully concluded on
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Topics Covered:
In a nutshell, during the webinar, our presenter – Anuradha Gore discussed the following topics:
- Introduction and Overview of Supplier Evaluation
- Understanding the requirements of ISO 13485 & 21 CFR 820 for Supplier Evaluation & Control
- How to do Supplier evaluation
- Documentation for Supplier evaluation
- FAQs
- Wrap up of the session
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.
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Hosted By
Sugandha Gupta
- Lead Strategy Consultant, MDV Freyr Solutions
Hosted By
Sugandha Gupta
- Lead Strategy Consultant, MDV Freyr Solutions
Sugandha Gupta is an accomplished Strategy Consultant specializing in the Medical Device, SaMD and IVD domains. Her commitment lies in delivering comprehensive end-to-end regulatory solutions, guiding organizations through complex compliance landscapes for successful market access and global expansion.
Sugandha excels in crafting tailored regulatory strategies that cater to the unique needs of healthcare industry stakeholders. She adeptly navigates organizations through intricate compliance requirements, ensuring seamless transitions and strategic implementations.
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Presented By
Anuradha Gore
- Senior Manager MDV, QMS team Freyr Solutions
Presented By
Anuradha Gore
- Senior Manager MDV, QMS team Freyr Solutions
Anuradha Gore, a seasoned Senior Manager at Freyr. With an overall experience of 18+ years in Biotechnology and Medical device industry, she serves as a QMS Subject Matter Expert, certified LEAs Auditor for ISO 13485, ISO 9001, and MDSAP.
Anuradha has an extensive experience with planning strategies and implementation of ISO 13485, ISO 9001, 21 CFR 820 and MDSAP with diverse portfolio of medical devices, IVDs and SaMD.