Learn how we sort results
Do you want to learn how we sort our results? Read more about how courses are ranked in the search results.
Relevance
Fundamentals of European Regulatory Affairs
PTI
|
Professional Training
4.8
(11)
-
Beginner level
-
From 1,895 GBP
-
London
-
Classroom
This course is designed to guide RA professionals through the necessary regulatory skills and understanding for optimising drug submission procedures....
Mastering Regulatory and Development Strategies for Generics
PTI
|
Professional Training
5.0
(1)
-
This course results in CPD hours
-
From 1,595 GBP
-
Multiple (2)
-
Classroom
Releasing a generic drug on the market can be fraught with regulatory challenges and compliance issues. This training course will...
Advanced Regulatory Affairs for Medical Devices
PTI
|
Professional Training
4.6
(5)
-
This course results in CPD hours
-
Advanced level
-
From 1,595 GBP
-
Multiple (3)
-
Classroom
The Medical Devices Regulation (MDR) was concluded in June 2016, which means significant changes for the European regulatory landscape for medical...
Regulatory, Developmental And Manufacturing Challenges For ATMPs
PTI
|
Professional Training
-
From 1,595 GBP
-
London
-
Classroom
This two-day course will provide you with a practical understanding of regulatory challenges, manufacturing concerns and clinical trial preparation for...
Regulatory Affairs Strategy
PTI
|
Professional Training
5.0
(2)
-
London
-
Classroom
This course has been designed to help you select the best registration strategy depending on the product area and indication....
Advanced European Regulatory Affairs
PTI
|
Professional Training
5.0
(1)
-
This course results in CPD hours
-
From 1,995 GBP
-
London
-
Classroom
Being a regulatory affairs professional in a pharmaceutical or biotech company is both challenging and rewarding. As a senior professional you must ensure...
Introduction to Regulatory Affairs for Medical Devices
PTI
|
Professional Training
5.0
(5)
-
This course results in CPD hours
-
From 1,595 GBP
-
Multiple (3)
-
Classroom
Following its ratification by the European Parliament, the Medical Devices Regulation will constitute major changes for the industry and is...
Displaying 1-9 of 9 results
Ads
