/    /  Basics on Regulatory Requirements in Clinical Research

Basics on Regulatory Requirements in Clinical Research

Book a session

Date Product Location Price  
06/09/2021 Basics on Regulatory Requirements in Clinical Research Brussels EUR 325.00 Book
06/12/2021 Basics on Regulatory Requirements in Clinical Research Leiden EUR 325.00 Book
thumbnail

About this course

Reasons to attend

Clinical Research is one of the most regulated industries in the world. Not a surprise, as we are dealing with research involving human beings. Therefore, safeguarding study participant’s rights, wellbeing and safety are of utmost importance. This is why before starting a clinical trial, you need to obtain appropriate approvals. Authorities and Ethics Committees play a major role in this approval process. This course is designed to provide a basic understanding of the current regulatory requirements for Clinical Trials for people who have limited or no background in these matters.

What's included?

  • Documents and materials related to this course are included
  • Globally recognised certificates awarded after test completion
  • This course has been granted PharmaTrain Recognition

Course schedule

  • Half a Day face-to-face training: 13h00-17h00


User registration

Reset Password