Featured Event
Get yours featuredMedical Devices: EU Regulations
$535*
E-Learning
At your desk
This course provides a solid understanding of medical device regulation in the EU. It covers the history of medical device regulation in Europe and follows the regulatory requirements throughout the product lifecycle.
Featured Event
Get yours featuredEssentials of European Medical Device Regulatory Affairs
£360
23 Jun 2020
Course
At Your Desk
Providing a basic, comprehensive overview of regulatory requirements and considerations for medical devices
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Get yours featuredGlobal Regulatory Strategy for Pharmaceuticals
$455*
E-Learning
At your desk
This course provides a basic understanding of the challenges and goals confronting a regulatory professional when defining a global regulatory strategy.
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Get yours featuredClinical Evaluation of Medical Devices
£1,700*
19 Jun 2020
Course
At Your Desk
This course will help you to understand the broad scope of clinical investigation and the regulatory processes required with the alternative routes to demonstrate compliance.
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Get yours featuredPharmaceutical Regulatory Affairs in the EU and US
£999*
E-Learning
At your desk
Nicholas Wells
A 9-module self-study course specifically designed for new entrants to pharmaceutical regulatory affairs wanting a complete overview of the issues and systems affecting the approval of their products.
Featured Event
Get yours featuredEssentials of European Pharmaceutical Regulatory Affairs
£580
06 Aug 2020
Course
At Your Desk
This course will provide a basic, comprehensive grounding in regulatory affairs
Featured Event
Get yours featuredEssentials of European Medical Device Regulatory Affairs
£360
12 Nov 2020
Course
Dublin
Ireland
This course will provide a basic, comprehensive overview of regulatory requirements and considerations for medical devices in a relaxed and interactive environment
Featured Event
Get yours featuredClinical Evaluation of Medical Devices
£1,700*
12 Jun 2020
Course
At Your Desk
This course will help you to understand the broad scope of clinical investigation and the regulatory processes required with the alternative routes to demonstrate compliance.