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Clinical Trials Monitoring Professional (CMPro) Health care and Pharmaceutical

Posted by samaa ahmed Sep 4

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About

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

The eligibility criteria for each organization may vary, but some common requirements are: Being at least 18 years old. Having a high school diploma or equivalent.

Completing a minimum of 40 hours of clinical research training. Being proficient in Good Clinical Practice (GCP) guidelines.

Having direct involvement in the care of at least 20 persons living with HIV within the last 36 months. Having no felony or drug-related convictions. Being in good standing with any state Board of Pharmacy.

Note: Eligibility requirements may vary based on the specific course or program you choose. Please refer to the detailed course brochure for more information.

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