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TGA Marketing Authorization Application, MAA submission, TGA Registrat

Freyr provides Regulatory Affairs services in Australia(TGA) for pharmaceutical products manufacturers during Marketing Authorization Application (MAA) Submissions, registration and entry into Australian Register of Ther
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CTD Dossier Template, Dossier Template, CTD templates, CTD Format

Freyr provides customized CTD dossier templates during preparing developing applications like MAA, IND, NDA, BLA, ANDA and IMPD in the CTD Format.
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What is Medical Device Ordinance (MedDO)?

The Medical Device Ordinance (MedDO) is a set of regulations applicable for the medical devices to be marketed in Switzerland align with the EU Medical Device Regulation (EU) 2017/745.
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Regulatory Submission Roadmap, Regulatory Intelligence, Regulatory Str

Freyr provides Regulatory Affairs Consulting Services during regulatory submission roadmap, regulatory intelligence, regulatory strategy, regulatory submission requirements and regulatory framework.
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Regulatory Strategy Consulting, Regulatory Consulting, Regulatory Affa

Freyr provides Regulatory Affairs support during the regulatory strategy consulting, regulatory consulting, regulatory affairs strategy, regulatory affairs consulting, pharmaceutical regulatory consulting services and re
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Health Authority Interactions, HA Queries, Pre-submission Meeting, HA

Freyr provides Regulatory Affairs support during the health authority interactions, HA queries, pre-submission meeting, HA requirements, health authority meeting, health authority requirements, pre-submission meeting req
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Global Regulatory Solutions Services Provider | Freyr

Freyr is a full-service global Regulatory Solutions and Services Company and a specialist provider of Regulatory Consulting, Operations Technology Services.
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Swixit - Regulatory Impact for Medical Devices Med Tech Industry

We are delighted to see your interest in Freyr’s Webinar Series (FWS). The webinar on “Swixit - Regulatory Impact for Medical Devices Med Tech Industry” was successfully concluded on March 23, 2022. Here is an archived
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Terms of Use

In June 2010, The Medicines Control Council (MCC) announced the intention to implement the South African Common Technical Document (ZA CTD) format which will replace the current MRF1 and any applications still in MBR1 fo
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Obligations for Economic Operators EOs | Freyr - Global Regulatory Sol

In June 2010, The Medicines Control Council (MCC) announced the intention to implement the South African Common Technical Document (ZA CTD) format which will replace the current MRF1 and any applications still in MBR1 fo
https://www.freyrsolutions.com/infographics/obligations-for-economic-operators-eos - Details - Similar

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