The EU Commission has published a new legislative framework package for the marketing and advertising of CE marked products on the European market.
Initial Cosmetic Webinar to Indie Beauty Members
The Obelis cosmetic regulatory team will present an introduction to the new EU cosmetics regulation at the Indie Beauty Network event in October 2011.
Code of Conduct for Notified Bodies?
The European Association of Notified Bodies for Medical Devices has published a new code of conduct in response to new EU medical device regulations.
EU Regulation & CE Marking Workshop in Sao Paulo, BRAZIL
Obelis and EG MONT announce new CE marking and EU regulatory workshop in Sao Paulo to discuss medical and in-vitro devices, cosmetics, and the WEEE directive.
Animal by-products EU regulation on Medical and Cosmetic products
Find out the definition of an animal by-product and what EU legislative guidelines apply to medical and cosmetic products containing them within the EU market.
EROMED Workshop in Sao Paulo a Success!
The two-day EU regulatory workshop included sessions on developments in medical device legislation and manufacturer obligations for the European market.
Medical Devices to Comply with the PPE 89/686/EEC
Under EU directive 2007/47/EC, PPE (such as masks and other safety equipment) must comply with medical device directive 93/42/EEC and PPE directive 89/686/EEC.
New Guidance on classification has been published
A new guidance document (MEDDEV) has been published on the classification of medical devices in Europe. Talk to Obelis' experts about your device's compliance.
Obelis launches “EROMED” Workshop
Obelis to host EROMED workshops in Israel in October 2009 to discuss EU medical device regulations and other EU compliance factors and requirements.
New package of measures for marketing of products
EU Commission revises 700 Old Approach directives and 27 New approach Directives. Read about these topics here.