Brookwood Global Online Training Brochure 2024

Contact us directly for the best group rates. • ONLINE TRAINING • GCLP Regs RM MD NIS CDM PV GDPR GCP Implementation of the EU Clinical Trial Regulation 2014 No. 536 (the CTR) began on 31 January 2022. It is important that both sponsors and investigators are aware of the significant changes and new requirements. Our four new on-demand, online courses offer training • for those needing a high-level overview • for those needing more in-depth knowledge • for investigator site members who need awareness of how the CTR changes their responsibilities and working practices. The courses are interactive, personalized using the participant’s 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 licence as ‘Scorm files’ to be delivered on their own learning management system. All of our CTR courses come with a link to our unique online bookshelf which contains useful documents relating to the CTR. This bookshelf is updated regularly and participants of courses have ongoing access to this. CTR for ALL – a high-level overview of the EU CTR This 15-20 minute course is ideal for those needing a short, high-level introduction to the EU Clinical Trial Regulation (CTR). It covers the main changes to working practices and highlights some of the new important requirements. Content includes: • When the CTR applies. • What the CTR brings that’s new. • Heads up on the new trial authorization process. • Significant changes to trial conduct. • Modifications, notifications and reports. • How the CTR affects the Trial Master File. EU CTR Click for product demo The EU Clinical Trial Regulation