Duration: (59:29) ?Subscribe5835 2025-02-23T08:48:56+00:00
EMEA Regulatory Changes and Corporate Landscape in the Region
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Regulatory Shorts#8 | How to get Marketing Authorisation in European Union (EU)? | Drug Registration
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EU Marketing Authorisation | What are the Steps and Timelines for Centralised Procedure at EMA?| DRA
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The EU's AI Act Explained
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Short course on the Medical Device Regulation (EU) 2017/745
(14:55)
Implementation of the clinical trials regulation
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EU Variation Overview Regulatory Lectures by Rajashri Ojha at Raaj Pharmaelearning
(1:24:57)
Type of variation filng in EU #variations #emea #guidelines #pharmaguide
(5:10)
Medical Device Regulation
(26:33)
What is the CHMP?
(2:28)
Marketing Authorisation in EU| European Medicines Agency (EMA)| MRP, DCP, CP \u0026 National Procedure
(11:4)
Introduction to the EU Regulatory System
(2:55)
EUROPEAN MEDICINES AGENCY I EMA I INTRODUCTION I HINDI
Future-proofing the EU’s medicine regulations
(3:3)
MARKETING AUTHORIZATION APPLICATION PROCEDURES | MAA | EUROPE | REGULATORY AFFAIRS
(23:7)
Why and how the EU regulatory system needs to evolve to be world-class?
(1:14)
A Day In the Life of... A Regulatory affairs director EMA
(22:4)
Regulatory pathways of Medical Devices in USA and European Union
(7:13)
Key EU Regulatory Developments in the Pharmaceutical Sector (2019-2020): Implications in Practice
(42:23)
US vs EU – Medical Devices Compliance and Regulatory Affairs
(5:51)