About the Clinical Research Certified Professional (CRCP)
This program has been designed to provide individuals seeking positions in the clinical research and pharmaceutical industry as a Clinical Research Certified Professional. A CRA assists in the design, preparation, planning, implementation and review of clinical trials according to ICH-GCP guidelines.
CRCP is a 15 weeks program offered twice in a year on Sundays from 09:00am to 1:00pm. It is accredited with 60 CME hours by DUHS. This course is facilitated by qualified professionals and is beneficial for Physicians, Pharmacists, Basic Health Scientists, Medical students, Nurses, and any other health professional seeking to enhance their knowledge in clinical research.
Program Highlights
Course Details
Course Outline
Admission Form
Processing Fee Voucher
Eligibility Criteria
Following is the eligibility criteria for admission cycle for Clinical Research Certified Professional (CRCP):
- MD/MBBS/BDS/FCPS
- Pharmacist
- Professional Nurses (R.N, BSN)
- B.Sc/M.Sc (Biological Sciences)
- Allied Health Sciences
- Students studying in 5th Semester or in 3rd year of MBBS/BDS/ Pharm.D or any other allied health Sciences disciplines (All Previous Semesters Cleared) are also eligible to attend the Course.
Learning Outcomes
At the end, the participants will be able to:
- Explore the latest advancements and best practices in clinical research
- Evaluate the compliance of clinical trials to regulatory requirements
- Compare various international regulations and best practices for the clinical research process.
- Describe the product development process through different phases of clinical trials.
- Identify the roles and responsibilities of the different positions thereby understanding the multitude of responsibilities that go along with clinical research leadership and how to apply them strategically in the clinical research.
- Explore the complex domain of research ethics and incorporate ethical practices in all stages of the clinical trial.
- understand and critically compare fundamental statistical and epidemiological concepts and methods
- Demonstrate an understanding and critically evaluate issues surrounding the risks and benefits of drug use in humans including the cause, manifestations and consequences of adverse drug effects (ADEs), how these are detected and monitored
- Construct documentation examples that are essential to clinical research.
Certificate Distribution Ceremony
Admission Process
Every stage of our admissions process is aimed at identifying the aspects of your academic trajectory and personal ambitions
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CLINICAL TRIALS UNIT