Overview

Life Sciences companies across the world require strong Regulatory support to make important decisions like expanding their product portfolio or to market their products across multiple geographies. En route, they face critical challenges while decoding local dossier requirements new guidelines, ingredient & claim analysis, labeling & packaging requirements, import regulations, local GxP requirements, etc. In such scenarios, there is an undeniable requirement to ensure that companies are aware of these existing geo-specific regulations and also of any forthcoming guidelines to be published. Then it becomes essential that companies need authoritative Regulatory Intelligence(RI), which can address all the challenges accurately.

With a robust network of local affiliates in more than 120+ global locations and in liaison with global Health Authorities (HAs), Freyr offers exclusive Regulatory consulting to address any Regulatory Intelligence (RI) query or requirement of companies across the globe. The team adheres to the best ethical practices as defined by RAPS & SCIPS, for collating Regulatory and market information from various sources.