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 The Medical Device Regulations? Read more about Obelis webinars on it.
Person Responsible for Regulatory Compliance: unveiling its meaning and role under the MDR.
Obelis expands monthly plan offering to include greater round-the-clock client support and EU regulatory consulting scope.
What does the new standard on Medical Device Regulation say.
The Obelis team visited Last Vegas in July 2018 to deepen relationships with clients, work on upcoming projects, and attend Cosmoprof North America.
As application designers have begun taking advantage of the advancements of technology and the growing patient trend for self-diagnosis and treatment, regulators have begun scrutinizing mobile medical apps.
The Obelis team visited Tokyo in May 2018 to develop relationships with clients and attend Beautyworld Japan, one of Japan's top cosmetics industry shows.
Understanding claims criteria and best practices for cosmetics products according to EU cosmetics regulation 655/2013: guidelines, compliance points, and more.
Working with a notified body is a mandatory obligation under the EU new approach directives. But how do you select the right one for your devices? We can help.