Freyrsolutions

Freyr provides Regulatory Affairs services in handling submission of CTA applications/Investigational Medicinal Product Dossier (IMPD) as per EU requirements for different types of medicinal products like New drugs, Recombinant Protein Products, Vaccines, Stem Cell-Based Products etc.

Freyr provides Regulatory Affairs services during planning, preparation and submission of Clinical Trail Application to comply with Health Authority Requirements.

Freyr provides end-to-end Regulatory Affairs services to the Biologics/Biosimilar product companies during BLA submission process, starting from pre-BLA/BPD meetings to further Life Cycle Management (LCM) of the various biological products.

Freyr is a Strategic Regulatory partner providing end-to-end Regulatory solutions and services to Innovator pharma companies during their innovator drug development process.

Freyr provides Swiss Authorized Representative (CH-REP) services to foreign medical device manufacturers for their product registration and market entry in Switzerland and acts as a single point of contact in the Country for liaison with Regulatory Agency.

Freyr provides End-to-End Regulatory Services in Malaysia to the pharmaceuticals, Medical Device, Food Supplements, and Cosmetic Companies to comply with NPRA Regulations.

Freyr iREADY is a technology based Cosmetic Ingredient Database platform and it provides Regulatory compliance support to manufacturers for cosmetics ingredients and management of product formulae in global markets.

Freyr provides End to End Chemical Regulatory Compliance services to health care consumers like product registration, notification, Formulation review and We offer EU REACH and CLP Registration/Dossier Update, Hazard Communication for quick market access.

Freyr Food Regulatory Affairs provides end to end regulatory support for Food/dietary supplements manufacturers in product notification, classification, and registration across the globe.

Freyr provides end to end Cosmetic Regulatory Services like formulation & ingredient review, label review, claims review, safety assessment & toxicology services, dossier compilation and market entry support.

Freyr acts as a Swiss Authorized Representative(CH-REP) on behalf of foreign medical device manufacturers during registration and compliant market entry of their products as per Swissmedic Regulations.

Freyr provides regulatory services and solutions in Mexico to comply with COFEPRIS for pharma, medical device, cosmetics and food supplement manufacturer companies.

Freyr provides Regulatory Software, Automation and Digital Transformation Solutions to support Global Lifesciences companies.

Freyr provides regulatory service in Canada to Generic medicine manufacturers/ANDS holders for preparation, review, and submission of Abbreviated New Drug Submissions (ANDS) as per Health Canada requirements.

Freyr helps Generic pharma manufacturers/ANDS holders in Health Canada (HC) interactions which include discussing and clarification of potential risks and issues related to their ANDS applications for fast approvals of generics drug products.

Freyr provides regulatory support in ANDS change control evaluation/assessment, post-approval submission strategy and preparation of change-related submission packages as per Health Canada requirements

Freyr provides regulatory support in managing and updating the Drug Master File (DMF) as per Health Canada guidelines and helps in Master file submissions in eCTD format.

Freyr provides regulatory services in Canada to Generic medicine manufacturers/ANDS holders in regulatory submission strategies for submission timelines, documents required for submission, approval process and registering generic medicine as per Health Canada requirements

Freyr provides regulatory services for the queries related to the sunset clause and understanding the guidance related to sunset clause.

Freyr provides Brexit regulatory services to Generic medicine manufacturers for those who are ready to market their products in United Kingdom (UK) and Europe (EU)