Knowledge Center

🔬 Discover the Future of Medical Device Regulation: Unveiling the QMSR Transition

 

Are you ready to navigate the evolution of regulatory compliance in the medical device industry?

Join us for an exclusive webinar hosted by Med-Di-Dia in partnership with Global Regulatory Services (GRS) as we unveil the groundbreaking shift from QSR to QMSR by the USFDA.

 

Dr. Shahram Ahmadi, renowned expert in medical device regulations, and Jacob Skinner, seasoned consultant at GRS, will lead you through this transformative journey.

 

📅 Save the Date: Thursday, June 27, 1pm to 2pm Irish Time

 

🔍 Key Highlights Include:

 

• Insider Insights: Gain a comprehensive understanding of the QMSR framework and its implications for your organization.
• Actionable Strategies: Learn practical steps to ensure seamless compliance with the new regulations.
• Expert Guidance: Benefit from the combined expertise of Dr. Shahram Ahmadi and Jacob Skinner as they share their industry knowledge and best practices.
• Interactive Q&A: Get your burning questions answered directly by our panel of experts.

 

🎯 Who Should Attend: RAQA consultants, Regulatory Affairs Managers, Quality Assurance professionals, and Medical Device manufacturers seeking to stay ahead of the regulatory curve and maintain compliance in a rapidly evolving landscape.

 

Watch Now

 

 

Don't miss this opportunity to future-proof your regulatory strategy and propel your organization towards success. Reserve your spot today for this exclusive webinar experience!

 

🔗 Wathch the recorded session Now: https://youtu.be/9REn_gQpKg0?feature=shared

 

Looking for Regulatory support? contact our experts mdd@mddltd.com or submit a web form via - https://med-di-dia.com/contact.php​ 

 

Stay ahead, stay compliant, and join us on the path to regulatory excellence!

 

 

Read More about QSR to QMSR by visiting - https://med-di-dia.com/news/iso-13485-for-usa-qsr-to-qmsr