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Pharma Regulatory Services in Spain
Freyr provides Pharma Regulatory Services in Spain for drug/biological product companies to support MAA Submissions, change in Market...
Pharma Regulatory Services in Sweden
Freyr provides Pharmaceuticals Regulatory Services to Sweden pharmaceutical companies to support in MAA Submission procedures (NP, MRP,...
Pharma Regulatory Services in UK
Freyr provides Pharma Regulatory Services in UK for Medicinal products companies to support in submissions & approvals of MAAs, Marketing...
Pharma Regulatory Services in Russia
Freyr provides Pharma Regulatory Services in Russia for Medicinal products companies to support in dossier submissions & compilation in...
Pharma Regulatory Services in Egypt
Freyr provides Pharma Regulatory Services in Egypt for medicinal products companies to support Drug registration, dossier submissions &...
Pharma Regulatory Services in Turkey
Freyr provides Pharma Regulatory Services in turkey for Medicinal products companies to assist with product development, market entry,...
Pharma Regulatory Services in Ukraine
Freyr provides Pharma Regulatory Services in Ukraine for drug/biological products companies to support Product registration, Import...
CFDA Mandates New Classification Catalog for Medical Devices
On August 1, 2018, China Food and Drug Administration (CFDA) - the Chinese health authority, has taken a major step towards...
Biosimilars in Europe and The USA: Decode Market and Regulatory Scenarios
Biosimilars, which are viewed as supplements for their equivalent biologicals in terms of safety, quality and efficacy (if & when...
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