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Freyr Solutions
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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
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
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
Freyr provides regulatory services and solutions in Mexico to comply with COFEPRIS for pharma, medical device, cosmetics and food supplement manufacturer companies.
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
Freyr SPL/SPM is cloud hosted and On-premise software that supports in electronic drug registration & listing management, Labeling Management, PI submission in SPL/SPM Format with Automated notification updates.
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 Australia provides End-to-End Regulatory Solutions & Services in Australia to the Pharma Innovator, Generics, Biologics, Medical Device, Food Supplements and Cosmetic Companies to comply with TGA 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 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. Freyrs artwork pack management services.
To understand the global outlook of biosimilars in terms of market and Regulatory perspectives, let us look at the market and Regulatory scenarios of biosimilars in two of the worlds biggest markets, the United States of America (USA) and Europe.
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 United Kingdom Responsible Person (UKRP) services to foreign medical device manufacturers in product registration and market entry in the UK and acts as a single point of contact in the Country for liaison with Regulatory Agency.
Freyr provides Global Regulatory Artwork Management Services; Solutions for life sciences Industry, which include Artwork proofreading, Artwork packaging, Artwork Lifecycle management, Artwork Studio Services.
Freyr provides regulatory and product registration support in Nigeria to comply with NAFDAC to pharma, medical device, cosmetics, and food supplement manufacturer companies.
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.
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 Regulatory services and solutions in Saudi Arabia to comply with SFDA regulations for pharmaceuticals, medical devices, cosmetics and food supplements manufacturing companies.
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.
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.
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.
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 Regulatory Software Solutions to support Global Lifesciences companies that include Pharmaceuticals, Medical devices, Cosmetics and Food Supplement companies to be complaint.
This article talks about latest ISO Revision on IDMP Implementation Guidelines & recent update of ISO/TS 19844, Implementation guidelines for ISO 11238 for data elements and structures for the unique identification and exchange of regulated informati
Freyr provides Regulatory Software, Automation and Digital Transformation Solutions to support Global Lifesciences companies.
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 provides pharmaceutical regulatory services in Italy for drug & biological product companies which spans across ASMF/CEP, MAA submissions via various procedures (NP, MRP, DCP & CP), dossier preparation, Product life cycle management as p
Freyr Solutions is a leading global Regulatory Solutions and Services company, serving more than 600 companies worldwide in the Life Sciences industry. With its presence in Thailand, Freyr offers end-to-end Regulatory, Labeling, and Clinical services to pharmaceutical, medical device, food, and cosmetic companies. Their expertise lies in areas such as Regulatory Affairs, Regulatory Operations, Labeling, and Market Access. Freyr's dedication to quality and customer satisfaction has earned them a reputation for being a reliable and trusted partner in the industry. Their commitment to innovation and compliance allows companies to navigate the complex regulatory landscape with ease and confidence.
Freyr provides food regulatory consulting support for Food/Dietary supplements manufacturers that span across product registration, Classification and formula review/ingredient assessment for compliant market entry of products across the globe.
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 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 Cosmetic Regulatory Affairs/Compliance Services for cosmetic industry that span across Product Registration, ingredient review, label and claims review, toxicology assessment and product information file for compliant market entry of product.
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.
Artwork creation requires a lot of coordination between designing studios, and quality check and review teams as well. With the teams situated at various locations, there exists a gap between teams and stakeholders involved in various stages of the p
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
Freyr SUBMIT Pro is one of the best eCTD software tool which helps Life science companies in various regulatory submissions to global health Authorities.
Freyr provides chemical regulatory compliance/management services for chemical industry that span across chemical registration/notification, toxicological assessment, compliance management and Data scouting services for compliant market entry of products.
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