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Freyrsolutions

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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.
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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.
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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.
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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.
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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.
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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.
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Contact Freyr for End-to-End regulatory services in Sri Lanka to comply with NMRA regulatory Requirements.
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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.
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Freyr provides medical device regulatory services in Sri Lanka during medical device registration, classification and licensing as per NMRA regulatory requirements.
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Freyr provides pharma/Medicinal product regulatory services in Sri Lanka as per NMRA during Medicinal Product Registration, Market authorization and Dossier Gap analysis.
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Freyr provides regulatory services and solutions in Sri Lanka to comply with NMRA to pharma, medical device, cosmetics and food supplement manufacturer companies.
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Freyr supports life science companies during Patient Support Applications, Pharmaceutical Press Releases, pharma advertising and avoid the issues of Prescription Drug Promotion (OPDP)
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Freyr is a dedicated global regulatory artwork services provider for Pharmaceuticals, cosmetics, medical devices and food supplements companies
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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
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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
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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
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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.
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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
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Freyr & team is specialized in creation of label content, tracking technical change specifications, creating artworks, managing artwork launch requests, integrating Regulatory text changes etc