It is important that both sponsors and investigators are aware of the requirements of the EU Clinical Trial Regulation 2014 No. 536

Our four on-demand, online courses offer training

• for those needing a high-level overview
• for those needing more in-depth knowledge
• for the investigator site members who need awareness of how the CTR changes their responsibilities and working practices.

The courses are interactive, personalized using participants name and have both narrated and read-only options.

On completion of these courses, participants are able to print a certificate of completion for their training records.

The courses are delivered using Brookwood’s Articulate Rise learning management platform. This allows participants to set their own password and access their training dashboard.

For group participation, we are able to track activity and provide progress and completion reports to the training organizers.

Alternatively, the course can be provided to organizations under license as ‘Scorm files’ to be delivered on their own learning management system.

Publications
We offer a uniquely indexed reproduction of the European Clinical Trial Regulation 2014  No. 536 as published in the Official Journal on 27 May 2014.
The unique Brookwood index of subject headings and key words helps users find the appropriate sections quickly and easily. The index also cross-references the Clinical Trials Directive 2001/20/EC, the Declaration of Helsinki and ICH GCP. Available in paper format in A5 and pocketbook and as an e-book