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.
News
Sanitary Certificates in Italy
In order to protect public health, shipments of goods of medical interest imported from third countries and arriving at the international entry points of the Italian territory are subject to controls by the National Medical Authority.
Read more on this topic here.
Implementing a GMP for Cosmetics
Learn more about the steps required to establish Good Manufacturing Practices for cosmetic products set for release on the European market.
Efficacy and Safety Claims: testing cosmetic products
Understanding claims criteria and best practices for cosmetics products according to EU cosmetics regulation 655/2013: guidelines, compliance points, and more.
Merger of Belgian IVD & MD authorities
Belgian medical and in-vitro diagnostic competent authorities merged in September 2017 for increased surveillance and traceability in devices on the EU market.
Registering Cosmetic Products in Spain
What is the process of registering cosmetic products in the Spanish market.
Medical apps under the new European MDR
Exploring the differences and between medical and well-being apps under the scope of EU medical device regulation 2017/745 and their legal requirements.
The new CE marking process for the Low Voltage Equipment
The new European Low Voltage Directive (LVD 2014/35/EU) outlines a new CE marking process for equipment on or to be introduced to the EU market.
(P) Steps to obtain CE Marking for your PPE 89/686/EEC Directive Products
Develop a roadmap towards obtaining a CE mark and compliance program for your PPE with Obelis' European Authorized Representative services.
The importance of GMDN Codes
According to the European Commission decision from 19th April 2010, uploading data into EUDAMED requires the use of GMDN codes. Read more on this topic.