The two-day EU regulatory workshop included sessions on developments in medical device legislation and manufacturer obligations for the European market.
Authorised representative (AR)
Obelis International Offices Convention
Obelis has launched its new International Offices and will be hosting EROMED at its home offices in Brussels, Belgium.
New Portuguese National Law Transposing the 2007/47/EC announced
As of March 2010, Portuguese national decree-law 145/2009 entered into effect, calling for the mandatory transposing of EU medical directives.
EUCORE Workshop: GMP – EN/ ISO 22716
Obelis to host EUCORE workshop in Israel on good manufacturing processes for cosmetics manufacturers looking to access the EU market.
EUCORE Workshop: The New European Regulation on Cosmetics
Obelis and Israeli Chamber of Commerce organise EUCORE event for cosmetics manufacturers looking to introduce products to the EU market.
EUCORE Workshop: GMP – EN/ ISO 22716
The EN/ISO/ 22716 guidelines are intended to provide guidance regarding Good Manufacturing Practices for cosmetic products. Find out what they include.
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.
Obelis launches “EUCORE” Workshop
Obelis to host EUCORE workshops in Israel in October/November 2009 to discuss EU medical device regulations and other EU compliance and regulatory factors.
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.