MDSAP Compliance and Audit Success

Medical Devices

Upcoming Webinar

March 07, 2024

45 Minutes

Join the Webinar as per your Time Zone

For AMR & EUA Regions

9:00 AM EST | 03:00 PM CET

For RoW Region

11:30 AM IST

What is it all about?

DYK? A significant number of medical device manufacturers still grapple with noncompliance issues, potentially jeopardizing patient safety. This ranges from complex compliance requirements to potential patient safety risks. The combination of inadequate documentation practices and the proliferation of non-compliant devices poses a significant threat.

Join our webinar on ‘MDSAP Compliance and Audit Success’ to explore the alarming issues manufacturers face, unravel the complexities of MDSAP compliance, and equip yourself with strategies to navigate the turbulent waters of global Regulatory compliance.

The webinar will be hosted by Pawan Sadhnani, and presented by Anuradha Gore. During the webinar, our experts will discuss the following:

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.
FAQs.

Given the keynotes and with due consideration for your hectic schedule, we look forward to seeing you in the webinar. Register now! Stay informed. Stay compliant.

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.