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Effectively Managing Vendor Oversight
PTI
|
Professional Training
4.9
(8)
-
This course results in CPD hours
-
From 1,595 GBP
-
London
-
Classroom
With robust structures in place, pharma companies are more successful at vendor selection, contract design, quality monitoring and risk minimisation...
Advanced Regulatory Affairs for Medical Devices
PTI
|
Professional Training
4.6
(5)
-
This course results in CPD hours
-
Advanced level
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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...
Clinical Research Project Management
PTI
|
Professional Training
4.7
(10)
-
From 1,995 GBP
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London
-
Classroom
As a complex and intricate process, the successful establishment and performance of clinical trials is reliant on a variety of...
Vendor Oversight
PTI
|
Professional Training
5.0
(2)
-
From 1,495 GBP
-
London
-
Classroom
Accurate and clear strategies for the monitoring of outsourced clinical trials has become more important than ever due to the...
Understanding Biocompatibility for Medical Devices
PTI
|
Professional Training
5.0
(2)
-
From 1,595 GBP
-
London
-
Classroom
Biocompatibility assessments are an essential part of submissions to regulatory agencies for medical devices. This course will provide you with...
Gaining Marketing Authorisations In CIS For Medical Devices
PTI
|
Professional Training
-
From 1,595 GBP
-
London
-
Classroom
With recent regulatory developments for medical devices in Russia, Ukraine and other CIS countries it is essential to remain up-to-date...
Health Apps and Medical Device Software in Europe
PTI
|
Professional Training
-
From 1,595 GBP
-
London
-
Classroom
This course offers a practical understanding of the European regulatory requirements applicable to medical device software, including a detailed overview...
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 1-8 of 8 results
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