Freyrsolutions

Freyr provides End to End Chemical Safety Regulatory Affairs (CSRA) services to consumer products manufacturers in product registration, classification, toxicology assessment, safety data sheet development and regulatory intelligence services as per region specific regulatory requirements for market approvals.

Freyr provides End to end regulatory support for food supplements manufacturers which include registration, classification and process clearances to comply with region-specific regulatory requirements for successful market entry of products across the globe.

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

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

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

Freyr provides Swiss Authorized Representative(CH-REP) services for medical device manufacturers outside the Switzerland as per Swissmedic regulations.

Freyr provides United Kingdom Responsible Person(UKRP) services for medical device manufacturers outside the UK as per MHRA regulations.

Freyr provides regulatory support to the medical device manufacturers in De-Novo registration of medical devices in the USA that span across classification, Pre-Submission/Q-Submission meeting request, risk benefit determination, De-Novo submission package compilation, publishing and creation for Pre-Submissions.

Freyr provides Swiss Authorized Representative(CH-REP) services for foreign medical device manufacturers and acts as Swiss distributor/importer of devices across Switzerland.

Freyr provides Swiss Authorized Representative(CH-REP) services for medical devices and IVD manufacturers in CE marking and labeling support as per Swissmedic regulations.

Freyr provides United Kingdom Responsible Person(UKRP) services for medical devices and IVD manufacturers that span across registration, UKCA marking, UK CE marking, UKNI marking and labeling support as per MHRA regulations.

Freyr provides United Kingdom Responsible Person(UKRP) services for foreign medical device manufacturers with end-to-end regulatory support for registration and market entry in UK.

Freyr provides regulatory support for medical device manufacturers in 513 g submission, which includes medical device classification, preparation & review of 513g application and interaction with agency to comply with CDRH, FDA.

Freyr provides regulatory support for medical device manufacturers in 510k submission (510 k premarket notification) to USFDA, which include predicate device identification, 510k application compilation, gap analysis, publishing, creation & validation of e-copy, device listing for compliant market entry.

Freyr provides cosmetic regulatory services in Brazil as per ANIVSA during cosmetic product registration, classification, Notification, formulation, claims review, CPSR and technical dossier compilation

Freyr provides food regulatory services in Brazil as per ANIVSA and CTCAF during food product registration, food classification, formulation, ingredient assessment, technical dossier compilation and submission

Freyr provides medical device regulatory services in Brazil during medical device registration, medical device classification and market entry as per ANVISA regulatory requirements

Freyr provides pharma/Medicinal product regulatory services in Brazil as per ANVISA during Medicinal Product Registration, classification, Market authorization and Dossier Gap analysis

Freyr provides regulatory services and solutions in Brazil to comply with ANVISA for pharmaceuticals, medical device, cosmetics and food supplement manufacturer companies