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ICH-GCP Certification

Online program is the most efficient way to provide consistent GCP training for your team members involved in any part of the clinical trials. Online training is extensively used by all global companies for providing regular training and updates to their team members.
Need of GCP Certification:
  • Global regulatory requirements
  • Key to conduct of ethical trials
  • Essential for clinical trials quality
Online GCP Certificate Program
CRQA offers GCP certification program for the clinical research, life sciences professionals, data management professionals and anyone involved in the clinical research. The program is offered both through Online and Workshop mode. Program covers the following key topics:
  • ICH GCP Principles
  • Ethical Considerations
  • Regulatory Compliances
  • Essential Documentation
  • Roles & Responsibilities of Key Stakeholders
  • Subject Recruitment & Retention
  • Monitoring
  • Quality Assurance
Duration
  • Duration of the Online Program is 1 Month.
  • Duration of the program could also be customized as per your needs
Who should take the course?
  • Investigators
  • Pharmaceutical companies
  • CRO staff
  • Research Institutes
  • Clinical trials support staff
  • Research Nurses
  • R&D staff involved in approving and monitoring clinical trials
  • Members of ethics committees
  • Graduates looking to develop
  • career in clinical research
Key Features
CRQA offers a state-of-the-art Online GCP training solution for the leading corporates. Our training features include:
  • Online 24x7 access to the training material
  • Online testing & certification
  • Real time training records management – this would save your important time of maintaining maintaining training records for audits and inspections
  • Detailed real time MIS for you to track the participant’s progress
  • Audio / Video or In person training by expert senior trainers at your facility
  • Flexible enrolment and bulk licence
  • Customisation of duration and content
  • Corporate identity
  • Duration and content of the program could also be customised as per your needs and target audience.
For more information and quote,
Please contact bd@crqa.in+91 98100 68241, +91 93111 72560

What's New
CRQA is looking for
qualified and Independent
Pharmacvovigilance Auditor
- experience essential in
Pharmacovigilance Audits.
Interested Professionals
may apply to bd@crqa.in
CRQA is looking for
qualified and Independent
Pharmacvovigilance Auditor
- experience essential in
Pharmacovigilance Audits.
Interested Professionals
may apply to bd@crqa.in
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