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The pioneers in Clinical research in India and world leading hospitals in the country -ICRI and Medanta; NH amd Max Hospital present PG Diploma Advanced Clinical Research, a 10 month job-oriented course.

A program devised by ICRI for you to train, experience and innovate at world class hospitals with international standards of technology and infrastructure. This is a unique platform to launch your career in Clinical Research and Healthcare.

Leaning centres are available at:

  • ICRI- Medanta Hospital, Delhi campus
  • ICRI- Max Hospital, Deheradun
  • ICRI- NH Hospital, Bengaluru & Jaipur Campus

Our award-winning  Post Graduate Diploma in Advanced Clinical Research programme was India’s first and till date the most sought-after programme within the science fraternity. ICRI has been a pioneering institution to introduce this programme since 2004 where more than 2,000 students have passed on our PG Diploma in Clinical Data Management making it the largest no of students in India to pass on this programme.

Course Objective

To provide participants with a broad understanding of the basic principles employed in diploma clinical research both domestically and internationally.

Course Content

Delivered through fourteen focused modules spanning over ten months.

  • Module I – Introduction to Clinical Research
  • Module II – Basic Pharmacology and Pharmacy in Clinical Research
  • Module III – New Drug Development
  • Module IV – Ethical Guidelines in Clinical Research
  • Module V – Ethics in Clinical Research
  • Module VI – Regulations in Clinical Research
  • Module VII – Biostatistics in Clinical Research
  • Module VIII – Specialist Clinical Trials and Clinical Trial Designs
  • Module IX – Clinical Trial Documentation
  • Module X – Quality in Clinical Trials
  • Module XI – Clinical Data Management
  • Module XII – Clinical Trial Management
  • Module XII – Drug Safety and Pharmacovigilance
  • Module XIV – Soft Skills for a Clinical Research Professional

Classroom teaching by eminent faculty involving Lectures and PowerPoint Presentations.

Assignments are given to students, which include preparation of CRF’s (Case Record Forms), IC (Informed Consent Forms), PIs (Patient Information Sheets), Protocol Designing, PMS (Post Marketing Surveillance Studies) plan designing.

Exercises are given to students wherein data on Toxicology, Bioavailability, Bio-equivalence is made available to the students and inferences, graphs and calculations are drawn from the same. Exercises are also in the form of MCQs (Multiple choice questions), Q&A (questions and answers) and Report writing.

Workshops are conducted for students emphasizing on problem-solving through interaction and exchange of information. Students have access to University's computer and internet Facilities enabling them in Data Searches and Computer-aided decision-making. Students have access to the Well-equipped library on Clinical Research with latest books, periodicals, newspapers, journals, prints and records are available for reading & reference.

Duration of course

10 months

Eligibility

Minimum eligibility criteria for application to the course would be either of the following:

MBBS/BAMS/BDS/BHMS/Physiotherapy and Occupational Therapy Graduates/B.Pharm/M.Pharm.

Graduates/ Post-Graduate Diploma In Clinical Research/Life sciences/ BioSciences with any of the following subjects-Chemistry, Botany, Zoology, Biochemistry, Microbiology, Genetics and Biotech with min 50%.

Admission Procedure

The admission process is fairly detailed & followed by Group Discussion and Personal Interview conducted by ICRI.