Greetings from Freyr Sri Lanka
Freyr is a global Regulatory leader providing services and solutions to Life Sciences companies in their entire Regulatory value chain. With our presence in 120+ countries, we help Life Sciences companies in their “local to global” journey. At Freyr Sri Lanka, we support companies to register their products with the NMRA, Regulatory strategy, market intelligence, in-country representation, PMS functions, and more. We also offer next-gen Regulatory software solutions covering the complete NMRA registration life cycle.
Freyr Expertise
- End-to-end Pharmaceutical Product Registration
- Authorized Local Representation
- NMRA Manufacturing Site Registration
- Sample Import License Support
- Query Support Management till Approval
- Pharmaceutical Lifecycle Management Support
- Ad-hoc Regulatory Affairs Consultation
Industries We Serve
NMRA is the key drug Regulatory Agency in Sri Lanka. The NMRA ACT, No. 5 of 2015 provides the authority to the NMRA to regulate and control the manufacturing, importation, storage, distribution, transportation, pricing, wholesale and retail sale, advertising and disposal of medicines.
- End-to-end registration support
- Authorized Local agent support
- Manufacturing site approval support
- Sample import license support
- Compilation and Submission of the dossier to the NMRA
- Query support management till approval
Freyr Digital
Freyr SUBMIT PRO, an eCTD Software, Suits All Your Submission Requirements
An Innovative, Cloud-hosted, AI/ML enabled Regulatory Intelligence platform offering a complete spectrum of authoritative Regulatory Information
Largest global ingredients repository and Regulatory database to support digitization of formulation assessment and real-time intelligence Know More
Freyr SPAR is one such RIM Solution that enables Life Science organizations to effectively manage the information right from tracking product registrations to generate statistical reports.
About Freyr
Freyr is a leading, niche, full-service global Regulatory Solutions and Services Company supporting, Large, Medium and Small size global Life sciences companies, (Pharmaceutical | Generics | Medical Device | Biotechnology | Biosimilar | Consumer Healthcare | Cosmetics | Chemicals) in their entire Regulatory value-chain; ranging from Regulatory Strategy, Support, Dossiers, Submissions etc. to Post- Approval / Legacy Product Maintenance, Labeling, Artwork Change Management and other related functions.
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