Description

Regulatory Courses

If you are a clinical research professional, investigator, monitor or other staff active in the field of clinical research and you need to understand and apply the laws of clinical trials conducted in Belgium, this webinar is for you. In about 1.5h all the new rules defined by the Belgian Clinical Trials Law of 07th May 2017, and what this means for procedures of clinical trials in Belgium, is presented on a comprehensive way. 

Complete Belgian Law

  

Belgium has taken the first preparative steps to be ready for the application of the European Clinical Trial Regulation 536/2014 by issuing a new clinical trials law. This law sets the new rules as well as paving the way for the legal basis of pilot studies in Belgium before the mandatory European Clinical Trials Regulation becomes effective. Many imperative changes are ahead, notably regarding procedures and ethics committees.

This webinar is designed for professionals who need to know the new Belgian Clinical Trials law of 2017. All the elements of the Law are presented in a clear-cut way. Specifics of the involved competent authorities, of independent ethics committees, of new submission procedures and timelines, of appeal after rejection of a clinical trial, of Phase I trials and centre requirements and of possible penalties. Adaptations to the current law of 07 May 2004 will be clarified and will enable you to get a clear view on what is applicable now and what is to be done in the future. In addition, procedures of the pilot studies are presented. 

The information will help you to understand upcoming Royal decrees and to avoid missing out on mandatory and specific Belgian legal aspects of clinical trials and of pilot studies conducted in Belgium.

  

Course time
13h30 - 15h00
Who should attend

Everyone involved in clinical research, including: Pharmaceutical companies, Contract Research Organisations (CROs), Investigators, Site Personnel.

People from clinical operations, regulatory affairs, quality assurance and pharmacovigilance departments involved in monitoring activities (on-site or medical monitoring) of investigational sites located in Belgium.

Everyone who wants to acquire knowledge of the Belgian Regulatory Requirements and who needs to comply to regulatory training requirements prior to performing work in Belgium.

 

After the webinar questions can be posted on the ECCRT Virtual Campus Discussion Forum.

  

Programme highlights
  • Introduction to and Scope of the 2017 Belgian Clinical Trials Law
  • Roles of the Competent Authorities FAMHP, College, Federal Authority of Health
  • Ethics Committees: The New Way
  • Procedures for Submissions
  • Specifications of Investigators and Phase I Investigational Sites
  • Requirements for Investigational and Auxiliary Products
  • Impact on the Clinical Trials Law of 2004
  • Pilot studies in Belgium

  

Learning Objectives
  • Acquire a clear view of all new rules of the Belgian Clinical Trials Law 2017 and understand its impact on the law of 2004.
  • Knowing the procedures to be compliant and reach successful clinical trials submissions in Belgium
  • Streamline the new requirements in your clinical research activities
 

  

Book a course

Date Lang Location
 
100,00 € excl. VAT (if applicable)

Testimonials

Brigitte De Witte
August 2017
Company
Sanofi

Very clear overview of the implementation in Belgium of the new EU CTR. Clarity and enthusiasm of the trainer. Practical exercises with voting possibility