Freyr provides regulatory and product registration support in Nigeria to comply with NAFDAC to pharma, medical device, cosmetics, and food supplement manufacturer companies.
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Freyr’s regulatory services in USA for Diagnostic Kits span across registration, notification and classification as per US FDA regulations to meet market entry requirements and fast track approvals for Covid-19 emergencies.
Freyr’s regulatory services in India for Diagnostic Kits span across registration, notification and classification as per CDSCO regulations to meet market entry requirements and fast track approvals for Covid-19 emergencies.
Freyr provides global regulatory services for Diagnostic kits span across registration, notification and classification in adherence with the regional compliance standards and fast track approvals for Covid-19 emergencies.
Freyr’s regulatory services in USA for Ultrasound Machines span across registration, notification and classification as per US FDA regulations to meet market entry requirements and fast track approvals for Covid-19 emergencies.
Freyr’s regulatory services in India for Ultrasound Machines span across registration, notification and classification as per CDSCO regulations to meet market entry requirements and fast track approvals for Covid-19 emergencies.
Freyr provides global regulatory services for Ultrasound machine span across registration, notification and classification in adherence with the regional compliance standards and fast track approvals for Covid-19 emergencies.
Contact Freyr for End-to-End regulatory services in Sri Lanka to comply with NMRA regulatory Requirements.
Freyr provides cosmetic regulatory services in Sri Lanka as per NMRA and CESC during cosmetic product registration, classification, Notification, formulation, claims review, CPSR and technical dossier compilation.
Freyr provides medical device regulatory services in Sri Lanka during medical device registration, classification and licensing as per NMRA regulatory requirements.
Freyr provides pharma/Medicinal product regulatory services in Sri Lanka as per NMRA during Medicinal Product Registration, Market authorization and Dossier Gap analysis.
Freyr provides regulatory services and solutions in Sri Lanka to comply with NMRA to pharma, medical device, cosmetics and food supplement manufacturer companies.
Freyr supports life science companies during Patient Support Applications, Pharmaceutical Press Releases, pharma advertising and avoid the issues of Prescription Drug Promotion (OPDP)
Freyr is a dedicated global regulatory artwork services provider for Pharmaceuticals, cosmetics, medical devices and food supplements companies
Freyr provides end to end regulatory artwork services & solutions for Cosmetics companies which include artwork management, artwork design & pack management, artwork studio and proofreading services
Freyr provides end to end regulatory artwork services & solutions for Food Supplements companies which include artwork management, artwork design & pack management, artwork studio and proofreading services
Freyr provides end to end regulatory artwork services & solutions for Medical device companies which include artwork management, artwork design & pack management, artwork studio and proofreading services
Freyr provides end to end regulatory artwork services for Pharmaceutical companies which include artwork lifecycle management, artwork design & pack management, artwork studio and proofreading services.
For Pharma Artwork staffing and artwork lifecycle management, Freyr has qualified Artwork Management professionals suiting to clients' onsite engagements which include Artwork Consultant, Artwork Designer, Artwork Proofreader/QC, Regulatory Affairs Associate for Labeling and Artwork etc
Freyr & team is specialized in creation of label content, tracking technical change specifications, creating artworks, managing artwork launch requests, integrating Regulatory text changes etc