Obelis expands monthly plan offering to include greater round-the-clock client support and EU regulatory consulting scope.
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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.
Obelis Group exhibited for the 13th consecutive year at Medica Trade Fair, one of the…
Obelis Group will hold an EROMED seminar at the MEDICA trade show, taking place from the 14th November till 17th November in Messe Düsseldorf, in Germany. The seminar, which is entirely free of charge, will be conducted at the Obelis booth (Hall 17, Stand D59), every day at 11 am and 3 pm. It will focus on the new proposal on EU legislation on Medical Devices and its impact on the compliance path and the CE marking process.
Obelis officially launched a new scientific department. It aims to aid manufacturers and help spread awareness around obligatory compliance issues.