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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
https://regulatoryaffairs.freyrsolutions.com/tga-marketing-authorization-application-maa - Details - Similar

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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Home - Apply for Canada eTA - Canada eTA

The Canada eTA (Electronic Travel Authorization) is a traveller verification system electronically linked to your travel passport, as an entry requirement for visa-exempt nations, while travelling to Canada by air.
https://canada-eta.com/ - Details - Similar

Experienced Environmental Engineers Consultancy Delhi, India - Green

Experienced Environmental Engineers Consultancy: Green Genra is platform for addressing the Environmental needs pollution control requirements of Industrial units by providing online Services Products.
https://www.greengenra.com/ - Details - Similar

eta canada visa application for tourist transit official for

eTA Canada Visa application Official - Get your electronic Travel Authorisation and evisa. formalities to tourist, transit or student - Apply Online here
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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.
https://regulatoryaffairs.freyrsolutions.com/ctd-dossier-templates - Details - Similar

Regulatory Labeling | Freyr - Global Regulatory Solutions and Services

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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Regulatory Affairs, Operations, Intelligence, Case Studies

Freyr s case studies on Regulatory Affaris and Operations, Regulatory intelligence, Submission and Publishing to FDA
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Swixit and Its Impact on the MedTech Industry

This article talks about the Swixit and its impact on the MedTech Industry and transitional timelines for various device categories.
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Swissmedic s New Medical Device Regulations

This article talks about the Swissmedic’s new medical device regulations for manufacturers to successfully market their products in Switzerland.
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