Freyrsolutions

Freyr provides Chemical Safety Consulting service to chemical and consumer companies in product hazard identification and risk assessment.

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 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.

Contact Freyr for Global End-to-end Food Supplement regulatory services to comply with Health Authority Requirements.

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

Freyr provides Cosmetics Regulatory Intelligence/Information services for product classification, registration, claims, labeling & Packaging requirements, local agent requirements and regulation across globe

Freyr provides compliant cosmetic claims review with Cosmetic Claim Substantiation, literature reviews and marketing claims to comply with regional health authorities

Freyr provides cosmetic product formulation and cosmetics ingredient review services to Cosmetic Companies across globe with regional and global safety regulations.

Freyr provides end to end Cosmetic Regulatory consultation support, starting from Regulatory intelligence to responsible person services for cosmetics and personal care companies 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.