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.

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.

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!

Speaker

Shahram Ahmadi
Med-Di-Dia
Dr. Shahram Ahmadi is a seasoned Regulatory Affairs and Quality Assurance Specialist, bringing 14 years of invaluable experience to our team. His expertise encompasses a wide spectrum of medical device categories, including implants, Personal Protective Equipment (PPE), and dermatological products featuring medicinal components. Shahram's proficiency shines through in his commitment to implementing ISO 13485:2016-compliant Quality Management Systems, developing Standard Operating Procedures (SOPs), and efficient audit management. Notably, Shahram has been a steadfast representative of Med-Di-Dia, actively participating as a speaker and delegate at various industry events, such as NSL Days, Medical Technology Ireland, and The Future of Swedish & Danish Life Science. He continues to be our distinguished ambassador in the Nordic Region.

Jacob Skinner
Global Regulatory Services
With a five-year background in UK and European Regulatory Affairs, he specialises in delivering comprehensive regulatory support to MedTech companies and medical device manufacturers. Jacob's expertise encompasses regulatory strategy and planning, ISO 13485:2016 Quality Management Systems integration, and medical device classification services. He hold