About the course: Good clinical practice (GCP) is an international quality standard provided by ICH, that helps governments in the development of local regulations for clinical trials involving human subjects. This course is based on the international ICH Good Clinical Practice regulations and is a complete training solution for all individuals that need to acquire GCP knowledge. It is suitable for anyone carrying out, or involved in, clinical research and clinical trials.
Duration: 1 month
Mode of Training: Distance
Eligibility:Graduate or Postgraduate in Life sciences/ Microbiology/ Biotechnology/ Pharmacy/ Medicine/ Nursing/ Physiotherapy/ Dentistry/ Homoeopathy/ Ayurvedic and Veterinary Science, Interns and Working Professionals.
1 To be able to understand the basics of Good Clinical Practice and the current legal regulations and guidelines
2 To have the confidence to identify and describe the main responsibilities of the IRB/IEC, the investigator, the sponsor and the monitor
3 To get familiar with the essential documents related to GCP and understand the essence and purpose of important trial related files such as the informed consent forms, the investigators brochure and the clinical trial protocol
Fees. USD 300/-