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Freyr provides United Kingdom Responsible Person(UKRP) services for foreign medical device manufacturers with end-to-end regulatory support for registration and market entry of devices in UK.
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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.
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Freyr provides UKRP services for foreign medical device manufacturers in acting as their UK responsible person and takes key responsibilities to meet MHRA regulatory requirements.
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Freyr provides United Kingdom Responsible Person(UKRP) services for medical device manufacturers outside the UK in MHRA registration and UKCA mark for their products.
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Freyr provides UKRP support during Medical Device registration with MHRA on behalf of the foreign manufacturer.
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Freyr acts as a United Kingdom Responsible Person (UKRP) for medical device manufacturers on their behalf for product registration and UK market entry
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Freyr provides post-Brexit regulatory scenarios for life Sciences manufacturers in UK & EU to be inline with new regulatory changes.
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Freyr provides Brexit regulatory services for life science companies in most Affected areas like Artwork/Labelling/Packaging, Clinical Trials, GMP, MRP/DCP National/Central Procedure, Pharmacovigilance and Trade Barriers.
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Freyr provides Global End-to-End post-Brexit regulatory services for Life sciences companies which include Pharmaceuticals, Medical devices, Cosmetics and Food supplements for compliant product market entry.
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Freyr provides End-to-end post-Brexit regulatory services in European Union for Life sciences companies which include Pharmaceuticals, Medical devices, Cosmetics and Food supplements for compliant product market entry.
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Freyr provides End-to-end post-Brexit regulatory services in United Kingdom for Life sciences companies which include Pharmaceuticals, Medical devices, Cosmetics and Food supplements for compliant product market entry.
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Freyr SUBMIT Pro is an cloud hosted, on-premise cost effective eCTD submission software with features like eCTD Submission tracker, Viewer, Validation and rDMS Integration.
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Freyr SUBMIT Pro is one of the best eCTD Submission software that suits all kinds of Regulatory eCTD publishing and submission requirements across the globe.
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Freyr SUBMIT Pro is an prominent eCTD publishing Software with various features like Inbuilt eCTD validator and viewer, submission tracking, HA query management, rDMS integration and many more.
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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.
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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.
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Freyr provides End-to-End Post Brexit regulatory support for Pharma, Medical Devices, Cosmetics and Food Supplements manufacturers who are willing to market their products in United Kingdom (UK) and EU.
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Freyr provides end to end regulatory support for medical device & IVD manufacturers in product registration, notification, classification across the globe.
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Freyr SUBMIT Pro is one of the best eCTD software tool which helps Life science companies in various regulatory submissions to global health Authorities.
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Various E-Learning Programs with connection to the co-learners and support of counsellors and coaches in Positive Psychology, Clinical and Counselling Psychology, Personal Development, and Leadership Coaching enables effective employee development and welfare.
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