- Conference
- May 2025
- 2 Days
Global
€1600EUR$1,742USD£1,299GBP
€1847EUR$2,011USD£1,499GBP
- Conference
- June 2025
- 2 Days
Europe
€1600EUR$1,742USD£1,299GBP
€1847EUR$2,011USD£1,499GBP
- Training
- December 2024
- 6 Hours
Europe
From €854EUR$898USD£717GBP
- Conference
- October 2025
- 2 Days
Europe
€1600EUR$1,742USD£1,299GBP
€1847EUR$2,011USD£1,499GBP
- Training
- September 2024
- 1 Day
Europe
From €1050EUR$1,105USD£882GBP
- Report
- February 2019
- 300 Pages
Global
From €4277EUR$4,499USD£3,593GBP
- Report
- August 2024
- 660 Pages
Brazil
From €3137EUR$3,300USD£2,636GBP
- Report
- August 2024
- 82 Pages
Japan
From €3327EUR$3,500USD£2,795GBP
- Report
- October 2023
- 171 Pages
Global
From €4278EUR$4,500USD£3,594GBP
- Report
- October 2023
- 172 Pages
Global
From €4278EUR$4,500USD£3,594GBP
- Webinar
- May 2023
- 360 Minutes
Europe
From €566EUR$595USD£475GBP
From €475EUR$500USD£399GBP
- Training
- 90 Minutes
Europe
- Training
- 90 Minutes
Europe
- Training
- 60 Minutes
Europe
- Training
- 60 Minutes
Europe
- Training
- 60 Minutes
Europe
- Training
- 60 Minutes
Global
- Book
- June 2024
- 496 Pages

The Clinical Trial Regulation market is a subset of the Clinical Trials industry, which is focused on the development and regulation of clinical trials. Clinical trials are conducted to evaluate the safety and efficacy of new drugs, medical devices, and other treatments. Clinical Trial Regulation is the process of ensuring that clinical trials are conducted in accordance with applicable laws and regulations. This includes the development of protocols, the selection of qualified investigators, and the monitoring of the trial. Clinical Trial Regulation also involves the review and approval of clinical trial data, as well as the reporting of adverse events.
Companies in the Clinical Trial Regulation market include Parexel, ICON, Syneos Health, PRA Health Sciences, and Quintiles. Show Less Read more