|Duration: 2 hours (the average time to complete the training program, including final assessments).
Credits Hours: 2
Self-paced Training: 24/7 access to course.
Enrollment Period: 3 months.
Demonstration: Try one of our FREE courses.
Certificate: View sample certificate.
THIS COURSE IS CURRENTLY NOT AVAILABLE.
Contact the BioPharma Institute for more information.
Training Program: GCP: An Introduction to Clinical Trials in India
Training Provided By: BioPharma Institute
Availability: Immediately available upon ordering.
Description: Online training with immediate access upon enrollment. India has been identified as an increasingly attractive country for conducting clinical trials and providing data management services. With its large patient population, well-trained investigators and considerably lower trial costs than in developed nations, India has gained wide recognition as a country capable of offering opportunities for conducting clinical trials. India’s rapidly evolving regulatory environment based on the fundamentals outlined by the International Conference on Harmonization (ICH) guideline for Good Clinical Practice (GCP) further enhances India’s reputation as a suitable location to conduct global clinical trials. This online course details the aspects of culture, custom and practice in India which investigators must understand in order to consider clinical trials in the country.
Certification Requirements: Students must view the entire program and successfully pass an online, multiple-choice final assessment with >80% passing grade within a 90 day period of time (180 days for Professional Certification Programs). Certificate is accessible in PDF format immediately after satisfying requirements.
Online Training Programs Include:
The GCP: An Introduction to Clinical Trials in India course is found in the following professional certification program(s):
Overview: This session briefly describes the legislative instruments that apply to the conduct of clinical trials in India.
Students completing this course should be able to: Outline the factors that make India suitable for conducting clinical trials. Recognize the global pharmaceutical sponsors’ concerns about conducting clinical trials in India. Review the opportunities and challenges for conducting clinical trials in India. Evaluate cost-effectiveness provided by clinical trials in India. Discuss the regulatory requirements which must be complied with when conducting clinical trials in India in order to license medicinal products in the EU and USA.
For more information on the BioPharma Institute’s training programs, or to suggest a course, please complete the form located below. Alternatively, you may call toll free in the US: (888) 4-BIO-LRN, international callers can dial (201) 301-8370, or email Support@BioPharmaInstitute.com.