Dr Shahram Ahmadi
Dr Shahram Ahmadi, Regulatory Affairs and Quality Assurance Specialist, Med Di Dia
Dr. Sharam Ahmadi is a seasoned Regulatory Affairs and Quality Assurance Specialist at Med-Di-Dia. With a successful track record spanning 14 years in the medical device industry, Shahram has extensive expertise in implants, PPE, and dermatological products featuring medicinal components. His adept-ness demonstrates dedication in advocating quality implementation of ISO 13485:2016-compliant QMS, along with developing SOPs and effectively managing audits.
Should Regulations Impact Market Entry for MedTech?
The regulatory landscape is constantly changing, making it difficult for start-ups to know where to start when launching their products internationally.
In this session, Dr. Shahram Ahmadi will share a proactive approach to market entry that sees regula-tions as an enabler, not a barrier.
Dr. Ahmadi will discuss the key factors to consider when launching a product in the EU and the US, and he will provide practical tips on how to navigate the regulatory maze.
Whether you're a start-up founder or a seasoned entrepreneur, this session is essential for anyone who wants to launch their product successfully in the global market.