Overview
Regulatory experts across 120+ Countries, offering localized Regulatory services for Bio-Pharma, Medical Device, Consumer Healthcare & Generic companies
Freyr’s global pool of Regulatory experts with a deep understanding of regional/local Regulatory requirements of 120+ countries enables Life Sciences companies to expand to new markets, in an accelerated model. Catering to the worldwide Regulatory needs, Freyr’s global capabilities span across Local Regulatory Affairs, Health Authority Interaction, Regional Regulatory Intelligence, Regulatory/Medical Writing (including local language documents), End-to-end submission & publishing, artwork & labeling, IDMP, CMC, QA/Audit Services etc.- pertaining to Medical Devices, Pharmaceuticals/Drugs, Cosmetics, Biologics/Biosimilars and Food Supplements.
Freyr’s balanced global presence includes:
