Featured Event
Get yours featuredClinical Evaluation of Medical Devices
£1,700*
05 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.
Featured Event
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.
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.
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
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 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.
Featured Event
Get yours featuredRAPS 2020 EURO Convergence
€1650*
26 Oct 2020 - 28 Oct 2020
Workshop
Brussels
Belgium
Focused on developing and sustaining a competent global regulatory workforce that drives good regulatory practice and policy to advance public health.
Featured Event
Get yours featuredIntroduction to Electronic Regulatory Submissions in the eCTD Format
$1,250*
20 Oct 2020 - 21 Oct 2020
Workshop
San Diego, California
USA
Do you need to comply with the impending electronic submission requirements for commercial INDs and Master Files?
Featured Event
Get yours featuredUnderstanding Clinical Development
£1,095 *
10 Jun 2020 - 12 Jun 2020
Course
At Your Desk
To provide an overview with practical advice from regulators and industry on the process of designing and conducting clinical trials
Featured Event
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.
