Blog | Freyr Solutions | Page 18 of 21

Labeling Requirements for Daily Chemicals in China

Drug Regulatory Affairs Freyr’s global Regulatory affairs expertise enables Life Sciences, Consumer Pharma and Bio-Med companies...

Regulatory Operations A Leading, Global, Regulatory Solutions & Services Company Supporting, Large, Mid & Small global Life Sciences...

Smarter the eCTD publishing software, smoother will be the eCTD submissions process. But to ensure the smoother submissions, life...

Freyr rDMS is an end-to-end electronic Regulatory Document Management system exclusively designed to enable Regulatory Groups and...

Freyr INSIGHT is Freyr’s Regulatory Intelligence Enterprise Platform, which gathers and analyzes publicly available regulatory...

Overview In an ever changing Regulatory environment, Regulatory authorities around the world mandate drug companies with various Drug...

Overview Audit & Inspection readiness – The first and foremost aspect every pharma company / a CRO should consider is the Trial Master...

Overview Beginning September 24, 2014 and going forward, all medical device manufacturers are required to meet the FDA mandated UDI...

The European Medicines Agency (EMA) is in the process of implementing the standards developed by the International Organization for...

Overview In the current trend of contract manufacturing across the world, drug product manufacturing is getting stringent and...