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Found 5726 results for any of the keywords marketing authorization. Time 0.007 seconds.

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.
https://www.freyrsolutions.com/what-is-meddo - Details - Similar

Regulatory Services - healthizalife

Our expertise areas include all segments of pharma product, food-dietary supplements and medical devices. We assist you with marketing authorization applications, such as those submitted under Directive, generic applicat
https://www.healthizalife.com/regulatory-services/ - Details - Similar

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

Global medicine database, Drug database and medicine price index

Largest global medicine database, drug database of Marketing Authorization medicines and medicine prices index. Ex-factory, wholesale and retail prices across 39 markets.
https://www.pharma14.com/ - Details - Similar

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
https://www.freyrsolutions.com/webinars/swixit-regulatory-impact-for-medical-devices-med-tech-industry - Details - Similar

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
https://regulatoryaffairs.freyrsolutions.com/health-authority-interactions-pre-submission-meetings - Details - Similar

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
https://regulatoryaffairs.freyrsolutions.com/regulatory-strategy-consulting-services - Details - Similar

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.
https://regulatoryaffairs.freyrsolutions.com/regulatory-submission-road-maps-regulatory-intelligence-services - Details - Similar

Regulatory Affairs, Operations, Intelligence, Case Studies

Freyr s case studies on Regulatory Affaris and Operations, Regulatory intelligence, Submission and Publishing to FDA
https://www.freyrsolutions.com/case-studies?tid%5B%5D=18 - Details - Similar

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