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Speaking Engagements

  

True Quality is a conference designed specifically for executives, quality, and regulatory professionals at high-performing medical device companies. The conference is also recommended for consultants, investors, and service providers. It is where the industry comes together to learn, network, and find inspiration.

06-08 June 2022
  

Bringing Competent Authority, Notified Body and industry experts together to discuss the evolving global regulatory landscape 9 focused tracks: EU MDR. IVD Regulation and Strategy. Software and AI. Legal and Compliance. Post Market Surveillance & Vigilance. Clinical Evaluations & Investigations. Global Market Regulations. Biocompatibility.

20-24 June 2022
  

The EU MDR 2017/745 was published in May 2017 with a transition period of three years which was extended by one additional year to address COVID 19 restrictions and limitations. This additional year was taken away from the predefined grace period in Article 120 of the EU MDR 2017/45.

27-27 September 2022
  

MEDICAL DEVICE REGULATIONS ACROSS THE GLOBE: YOUR DEDICATED HUB TO ACHIEVING COMPLIANCE Combining FDA, Notified Body and Industry Perspectives to Shape the Future of Medical Device Regulations 4 Tracks across 3 days: Medical device regulation and implementation. Biocompatibility. Software and AI for Medical Devices. In Vitro Diagnostic Regulations.

06-08 December 2022