Freyr is a trusted partner, providing end-to-end Regulatory services, across Top 20 global brands for 6 of the Forbes* Global Top 10 Fortune 500 Healthcare/Life Sciences, Mid-market $1+ Billion Bio Pharma, and Several Small-Medium, Life Sciences Comp

Freyr Artwork Pack Management CoE provides innovative, cost-effective, and creative graphic design & artwork services to support new product launches and brand re-designs for global lifesciences companies. Freyr’s artwork pack management services.

Freyr team has exposure to Pharmaceutical Artwork Product lifecycle management/PLM tools which spans across Centralization of end-to-end artwork process, Audit-trail management, 21CFR compliant, GMP compliant, Safety label changes.

Freyr helps API Manufacturers in CEP compilation, review & submission to EDQM for all types of APIs as per EDQM guidelines for approval of MAAs/ANDS. CEP adds an advantage for API manufacturers while entering the EU CEP to the monographs.

China Food and Drug Administration (CFDA) - the Chinese health authority, has taken a major step towards classification of medical devices to be marketed or currently being marketed in China. The CFDA has officially published and mandated the new Med

We offer Clinical Trial Auditing & Monitoring services for both the clinical and bio-analytical phases of the Bioequivalence (BE) studies & Bioavailability (BA) studies, Clinical SOP preparation & review as per ICH GMP, US FDA, EMEA, ANVISA.

We offer clinical protocol preparation and review services, Clinical Trial Audit & Monitoring Services for clinical & bio-analytical phases as per the specific standard like ICH GCP, USFDA, EMEA, ANVISA regulations.

Freyr tailors solutions to meet a variety of medical writing needs with respect to clinical trial services starting from strategic services for the conduct of clinical trials till the submission of clinical trial dossier, compilation and review of pr

Freyr helps cosmetic companies with Cosmetics Classification, Notification/Registration in Australia, Ingredient Analysis, Label assessment, Claims Review & Consultation as per TGA regulation for cosmetic products under the NICNAS & ICNA Act.

We help cosmetic companies with Cosmetics Classification, Registration in Canada, Ingredient Analysis, Label Assessment, Claims Review & Consultation, Label Translation, Notification as per Health Canada (HC) under Food and Drugs Act and Cosmetic

Freyr helps cosmetic companies in Mexico with Cosmetic Classification, Registration in Mexico, Formulation Review, Claims & Substantiation Services, Labeling Review, Import license acquisition, Consulting & Renewal Services as per COFEPRIS reg

We help cosmetic companies with Cosmetic Registration in Nigeria, Formulation Review, Notification Holder, Claims & Substantiation Services, Labeling Review, Product Information File (PIF) Compilation, MOH Audit Consultancy, Renewals as per NAFDA

Freyr helps cosmetic companies with Cosmetic Registration in Russia, Formulation Review, Notification Holder, Claims & Substantiation Services, Labeling Review, Product Information File (PIF) Compilation, MOH Audit Consultancy.

We help cosmetic companies with Cosmetic Classification in Saudi Arabia, Formulation Review, Claims Review, Labeling Review, Translations, eCOSMA Registration/Notification, Legal Representative, Distributor & Import Services as per SFDA regulatio

We help cosmetic companies with Cosmetic Notification in South Africa, Formulation Review, Claims & Substantiation Services, Labeling Review, Product Information File (PIF) Compilation, Notification Holder, MOH Audit Consultancy, Renewals.

We help cosmetic companies with Cosmetic Classification, Registration in USA, Artwork Support, Ingredient & Label Assessment, Claims Review, Product Notification through Voluntary Cosmetics Registration Program (VCRP), PIF Compilation, Import Service

Freyr provides Pharma Regulatory services in Austria for pharma manufacturers which spans across strategic support on MAA procedures, pre-submission activities in eCTD format, dossier compilation, post-approval changes & lifecycle management as per E

Freyr provides Pharma Regulatory Services in Belgium to Drug & biological products companies which includes MAA Submissions in eCTD format, selection of the RMS & CMS, ASMF/CEP, dossiers Submissions to HAs, post-approval support as per Federal Age.

Freyr provides Pharma Regulatory Services in Czech Republic to pharmaceutical manufacturers which spans across MAA Submissions, dossier submissions in eCTD format, QPPV, post-approval support, interaction with HAs as per EU Regulations.

Freyr provides Pharmaceutical Regulatory Services in Denmark to Medicinal Product companies which includes Product registration, MAA Submissions, lifecycle management, HA query response, variation submissions & license renewals as per EMA Regulat