About Course

A Clinical Trials Monitoring Professional (CMPro) course is a program that trains clinical research associates (CRAs) to monitor, supervise, and support clinical trials in accordance with good clinical practice (GCP) standards and prepare you for the exam offered by the Biopharma Institute.
The CMPro course covers topics such as:

  • ICH-GCP Good Clinical Practice.
  • Clinical Trial Monitoring: Site Evaluation and Set-up.
  • Clinical Trial Monitoring: Documentation and Closure.
  • Clinical Trials: Preparation and Design.
  • Clinical Trials: Preparing for an Audit or Inspection.



Eligibilities

--- Health care and Pharmaceutical ---

Clinical Trials Monitoring Professional (CMPro)

Total Days
26 Days
Total Hours
170 Hours
Training Mode
Price


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Online BootcampPreferred
  • Flexi Pass Enabled: Flexibility to reschedule your cohort within first 90 days of access.
  • Live, online classroom training by top instructors and practitioners.
  • One year access to high-quality self-paced eLearning content curated by industry experts.
Classroom TrainingPreferred
  • Customized Training Solutions: Tailor classroom sessions to your team's needs, with options for instructor-led or blended learning formats.
  • One year access to high-quality self-paced eLearning content curated by industry experts.
  • Interactive Learning Environment: Engage with a simple, interactive setup that encourages active participation and hands-on learning.
Corporate Training
  • Customize the learning model according to your team's needs. Get digital material, instructor-led classes or both.
  • Get flexible pricing options according to your company's needs.
  • Simple and interactive Learning Management System (LMS).
  • Enterprise dashboard for individual learners or teams.
  • Learner support and assistance available 24/7.
  • One year access to high-quality self-paced eLearning content curated by industry experts.


Documents