Contact us directly for the best group rates. info@brookwood-global.com • ONLINE TRAINING • GCLP Regs RM MD NIS CDM PV GDPR GCP Modern, exciting online, on-demand course covering the Good Clinical Practice (GCP) requirements of both sponsors and the investigator site. • Based on ICH GCP Guidelines E6(R2). • Needs no prior knowledge of GCP. • Ideal as core basic training. • Suitable as a GCP refresher for sponsor and investigator site personnel. • A great course to provide GCP knowledge to those assisting with clinical trials, administrators, ethics committees and regulators. • Complete eight main sections to reach a final test. – GCP Essentials and Principles – Pre-study Activities – Protocol and Trial Conduct – Participant Protection and Safety – Data Quality and Reliability – Risk Management and Trial Monitoring – Documentation and Trial Files – Audit, Inspections and Closure • Narrated, or read-only. • Takes around 2 hours – stop and start at any time. • Interactions and quiz questions to maintain interest. • Personalised with first name. • Additional resources form part of the course including e-books entitled ‘Essential GCP’, ‘Indexed ICH GCP Guidelines’, ‘A Guide to Informed Consent’ and ‘Risk Management in Clinical Trials’. • Pass the final test (80% or more) to be awarded certification. • Opportunity to repeat incorrectly answered questions in the event of a test score lower than 80%. • Available as fully serviced training (registration, activity monitoring, progress reporting, certification, helpline) or run it on your own learning management system. TransCelerate 4 Regs MD RM PV GCP GDPR GCLP NIS CDM GCP Click for product demo FLAGSHIP ONLINE COURSE Fundamentals of GCP
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