Education/Interactive Workshop on Good Clinical Trial Practices (GCP)

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Good Clinical Practice (GCP) is the gold standard for conducting clinical trials involving human subjects. It encompasses ethical and scientific quality benchmarks that protect participants’ rights, ensure safety, and enhance the credibility of data.

This one-day interactive workshop introduces participants to the foundational and operational elements of GCP, including trial design, documentation, data handling, and participant protection. Emphasis is placed on aligning with global guidelines and improving the quality of clinical trials conducted in India.

This programme aims to:

  • Familiarise participants with international GCP guidelines and their application
  • Enhance understanding of ethical considerations and participant rights
  • Guide researchers and ethics committee members in maintaining data integrity and safety oversight
  • Promote standardised practices for clinical trials across healthcare institutions
  • Build capacity within institutions to meet global clinical trial expectations

This training is ideal for:

  • Clinical Research Professionals
  • Investigators and Co-Investigators
  • Contract Research Organisation (CRO) Staff
  • Ethics Committee Members
  • Clinical Trial Coordinators and Nursing Professionals involved in research
  • Quality and Compliance Officers involved in trial monitoring

NABH recommends that institutions nominate professionals from multiple departments to encourage unified and ethical clinical research practices.

  • INR 4,000 + GST @ 18% = INR 4,720 (Total)

The fee includes:
• Access to the full virtual workshop
• Course materials and reference documents
• Certificate of Participation (subject to full attendance)

Please note: The fee is non-refundable and non-transferable.

Quality Connect Training with NABH

Type

Paid program ₹4720

Venue

This session will be conducted live via a digital platform, enabling participation from any location.

Program duration

1 day

Date(s)

28.09.2025

Time

2:00 pm to 6:00 pm4 hours

This one-day session is designed to be intensive and interactive, suited for professionals involved in clinical research and trial governance.

Total seats

(Seats are limited and will be allotted on a first-come, first-served basis.)

Other Information:

For any further assistance or queries, please write to us at training@nabh.co


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