Regulatory services in Sri lanka
- Freyr Global Regulatory Solutions
- Sep 19, 2017
- 1 min read
Aiming at diversification of medicinal products and medical devices manufacturing base, Sri Lanka offers good business opportunities for Pharma, Biogen and Generic product manufacturers. For the market entry, however, the new entrants are obliged to obtain approvals from Cosmetics, Devices, & Drug Regulatory Authority (CDDA). Only drugs/devices registered and compliant with the authority standards can be manufactured, imported and marketed for sale in the region. Lack of updated Regulatory knowledge may sometime challenge or restrict manufacturers’ compliance efforts.
Freyr Provides Regulatory services in Sri lanka
With an expert Regulatory affairs consulting team, Freyr assists manufacturers to decode the complex Regulatory requirements in the region and help them navigate the procedural challenges in time for successful market authorizations. Freyr’s Regulatory services in Sri Lanka span across:
Pharmaceutical
Cosmetics
Veterinary
Kommentare