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Certificate

Good Clinical Practices

Program code:

Credential:

Certificate

Duration:

Delivery Mode:

Start Date(s):

January | May | September
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Program Overview – Good Clinical Practices (GCP)

Good Clinical Practices (GCP) training is essential for professionals working in clinical research and is widely adopted by hospitals, universities, academic medical centers, and healthcare companies. This training ensures ethical conduct, data integrity, and regulatory compliance in clinical trials. Professionals with expertise in GCP are highly sought after across the healthcare, pharmaceutical, and biotechnology industries.

After successful completion of this course, students will be:

  • Able to understand current good clinical practices
  • Able to organize clinical studies
  • Able to coordinate clinical studies
  • Able to write procedures and protocols
  • Able to perform audit and inspections

  • GCP regulatory requirements
  • GCP in clinical studies

  • GCP in protocol development processes
  • GCP in various clinical study activities
  • GCP in clinical studies

  • GCP for Clinical Trials with Investigational Drugs and Medical Devices (U.S. FDA Focus)
  • GCP for Clinical Trials with Investigational Drugs and Biologics (ICH Focus)

Who Should Attend

Anyone who wants to become the following should attend this webinar on good clinical practices:

  • Clinical Research Associate
  • Research Professionals
  • Healthcare Professionals
  • Clinical Research Associates
  • Clinical Research Coordinators
  • Clinical Research Project Managers
  • Auditors and Inspectors