Freyr provides end-to-end regulatory services for medical devices manufacturers in Europe to comply …
Freyr provides regulatory support for medical device manufacturers in classification of their produc…
Freyr provides regulatory support for medical device manufacturers in 510k submission (510 k premark…
Freyr provides regulatory support for medical device manufacturers in 513 g submission, which includ…
Freyr acts as an authorized representative(AR) on behalf of the foreign medical device and In-Vitro …
Freyr acts as a local authorized representative (AR) on behalf of foreign medical device manufacture…
Freyr provides US agent representation services for medical device manufacturers and serves as a lia…
Freyr acts as a European Authorised Representative (EAR/EC REP) for foreign medical device manufactu…
This article talks about the Japan’s Consumer Affairs Agency (CAA) revised labeling standards for fo…
This article talks about the Health Canada's Regulatory standards and authorization pathways for fac…
This article talks about the FDA’s final guidance on multiple function device products’ pre-market r…
This article talks about the MHRA (Medicines and Healthcare products Regulatory Agency) issued post …
This article talks about the Mexico’s COFEPRIS (The Federal Commission for Protection against Sanita…
Couple of months back we thoroughly discussed about FDA’s expedited Regulatory pathways during medic…
MHRA has published guidance on the new rules that will govern the regulation of medical devices and …
It is a known fact that the UK has officially left the European Union (EU) on January 31, 2020 and i…
As we all aware, COVID-19 pandemic resulted in the suspension of regular on-site inspections and as …
This article talks about the EMA’s temporary updated guidance on GMP(Good Manufacturing Practices) a…
Freyr’s Generics Regulatory services support clients with Regulatory strategy, lifecycle management,…
Biological medicinal products are promising solutions in the prevention and treatment of several lif…
Freyr provides pharmaceuticals Regulatory affairs services enable Life Sciences, Consumer Pharma and…
The article talks about the EMA published a revised guidelines on the quality of water used for phar…
This article talks about Australia’s new update on implementing a ban on the usage of animal test da…
This article talks about the China’s NMPA published final version of Cosmetic Supervision and Admini…