On the 24th of April 2020, Regulation 2021/561 was adopted and published, delaying the MDR by 1 year to May 26th 2021;
But what did this mean for Medical Device manufacturers?
Our FREE Webinar was to find out and hear about the MDR DELAY EXPLAINED – we covered the impact on:
Obelis Academy held the webinar MDR Delay: what has changed on May 27th, 2020. Bottom line: 1-year delay provides you with additional time to finalize your compliance with the MDR, which was a complex and lengthy process!
Obelis Academy organized COVID-19 Webinar – Cosmetic on April 29, 2020.
The webinar was especially designed to teach you, step-by-step, how to place on the EU Market Covid-19 related cosmetic products, with a special focus on hand sanitizers (classified as Cosmetics or Biocides).
The aim of this online comprehensive course was to provide the knowledge and train attendees to be able to act as “Person Responsible for Regulatory Compliance” within their organisations under the Medical Device and In-Vitro Diagnostic Regulations (MDR & IVDR).
Interested in other webinars? Let us know!
Interested in The Medical Device Regulations? Read more about Obelis webinars on it.
Updates & Implementation on Medical Devices Regulations
Are you interested in the Medical Devices Regulations? Check out our webinars on these topics.
Due to the outbreak of the Covid-19 in Europe, the European Union was registering increasing shortages of test kits and IVD-related devices.
Our FREE Webinar was to find out and hear about how to register IVDs in Europe.
Person Responsible for Regulatory Compliance: unveiling its meaning and role under the MDR.