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Introduction to Pharmaceutical Regulatory Affairs (Spring edition)
The Organisation for Professionals in Regulatory Affairs
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Professional Training
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From 3,010 GBP
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01/03/2025
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Online
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Self-Paced Online
TOPRA's Introductory Courses have been designed to provide a firm foundation to your career in regulatory affairs. It is the...
Regulatory Information Management & IDMP Training
PTI
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Professional Training
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From 1,595 GBP
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London
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Classroom
Over two days you will learn the key aspects of RIM and the new IDMP standard such as training and...
Introduction To Regulatory Affairs In The MENA Region
PTI
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Professional Training
5.0
(2)
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Beginner level
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From 1,400 GBP
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Online
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Virtual Classroom
Using a combination of theory and practical case studies, this course will allow participants to develop the knowledge needed to...
Essentials of European Pharmaceutical Regulatory Affairs
The Organisation for Professionals in Regulatory Affairs
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Professional Training
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From 580 GBP
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Online
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Self-Paced Online
This course will provide a basic, comprehensive grounding in pharmaceuticalregulatory affairs in a relaxed and interactive environment. This popular course...
European Regulatory Procedures
The Organisation for Professionals in Regulatory Affairs
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Professional Training
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From 1,095 GBP
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Online
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Self-Paced Online
A course designed for individuals involved in developing European regulatory strategies for projects or wishing to gain the knowledge and...
Essentials of European Regulatory Affairs (Online Course)
The Organisation for Professionals in Regulatory Affairs
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Professional Training
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From 340 GBP
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Online
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Self-Paced Online
The world of Regulatory Affairs can be a confusing and complex place, particularly if you have no formal industry background....
Pharmaceutical Regulatory Affairs in China
PTI
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Professional Training
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From 1,200 GBP
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Online
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Virtual Classroom
Develop or market your drug in China more effectively with a deep understanding of the Chinese pharmaceutical regulatory landscape. In...
Regulatory Guide to the Generics Market
PTI
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Professional Training
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From 810 GBP
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Online
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Self-Paced Online
Bringing a generic drug to market can be fraught with regulatory challenges and compliance issues. Alongside the high amount of...
Introduction to EU Regulatory Affairs
PTI
|
Professional Training
5.0
(5)
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From 1,200 GBP
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Online
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Virtual Classroom
This introductory course will provide you with a grounding knowledge of regulatory affairs in Europe. After three days you will...
Fundamentals of the EU IVD Regulation
PTI
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Professional Training
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From 999 GBP
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Online
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Self-Paced Online
The in-vitro diagnostic sector has undergone a regulatory transformation, similar to that seen in medical devices. Under the existing Directive,...
Fundamentals of European Regulatory Affairs
PTI
|
Professional Training
4.8
(11)
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Beginner level
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From 1,895 GBP
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London
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Classroom
This course is designed to guide RA professionals through the necessary regulatory skills and understanding for optimising drug submission procedures....
Optimising Regulatory Strategies for Orphan Drugs
The Organisation for Professionals in Regulatory Affairs
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Professional Training
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From 675 GBP
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Online
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Self-Paced Online
This CRED course will provide a comprehensive understanding of the opportunities and challenges offered by orphan drug regulations and practical...
Post Market Surveillance and Vigilance Requirements for Manufacturers (EU 2017/745)
NSF International, Health Sciences
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Professional Training
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From 299 USD
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Online
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Self-Paced Online
Post-market surveillance for manufacturers is covered in Articles 83-86. Articles 87-89 cover post-market vigilance requirements. This course reviews the requirements...
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