GCP Training & Education
ClinicalRM offers preclinical and research training to meet various client needs. We provide trainers with experience in the conduct of Government and Industry managed trials. Our trainers have functioned as coordinators, CRAs, and Principal Investigators (PIs), managed quality assurance units, directed regulatory compliance programs, and manged multiple clinical trial and data management centers. The scope of the training and experience provided includes both Investigator and Sponsor responsibilities. We provide 1:1 mentoring, on-site and off-site seminars, and conferences of all sizes, and ensure precise planning, logistical management, and execution of all sessions. Our creative an varying approaches include a focus on ensuring a high level of assimilation of content. ClinicalRM’s training offerings include both standard modules and customized trainings offered in a multitude of vehicles to meet the customers’ needs. These range from webinars, workshops, and 1-2 day GCP coferences.
We have previously offered the following training and education courses, but can arrange custom courses to suit your specific learning needs.
- • 21 CFR Part 11
- • Construction and Maintenance of the TMF
- • Saftey Reporting
- • Clinical Data Management
- • Source Documentation for Informed Consent
- • Project Management for Sites and Sponsors
- • CRA Training
- • Data Safety Monitoring
- • Essentials of Clinical Trails
- • FDA Inspection Preparedness
- • GCP Basic and Advanced