PGDCRP
Course objective
- To give learners a thorough understanding of the fundamental concepts used in clinical research diplomas both domestically and worldwide.
- We will concentrate mostly on pharmacy graduates because there aren’t many of them working in the clinical research sector.
- The number of students will determine the length of the course.
Modes of PGDCRP Course
Mode 1 (Certification Course)
- PGDCRP (Certification Course) Duration 6 Month
Course Module & Doubt Classes Provided Online - Fees: 21,000 INR
Mode 2 (Online Course)
- PGDCR (Online Classes) Duration 9 Month (6 Month Online Classes + 3 Month Onsite Training )
- Fees: 35,000 INR
- Timings: Monday to Friday (10AM-11AM, 1PM-2PM, 4PM to 5PM or Saturday Sunday (10AM to 1PM)
Mode 3 (Online + Onsite Training Course)
- PGDCR (Online Classes + Onsite Training) Duration 9 Month (3 Month Online Classes + 6 Month Onsite Training )
- Fees: 50,000 INR
- Timings: Monday to Friday (10AM-11AM, 1PM-2PM, 4PM to 5PM or Saturday Sunday (10AM to 1PM)
Mode 4 (100% Onsite + 100% Placement Course)
- PGDCR (100% Onsite Training + Placement) Duration 9 Month (9 Month Onsite Training with Classes)
- Fees: 90,000 INR
- Timings: Monday to Friday (10AM to 5PM)
What is the scope after Completion of PGDCR?
- After completion of post graduate diploma in clinical and pharmacovigilance, you can work in Clinical Research Industry as a –
- CRA (Clinical Research Associate), Biostatisticians
- CRM (Clinical Research Manager)
- CDM (Clinical Data Manager)
- Clinical Research Coordinator,
- Regulatory Affairs Manager (RAM),
- Pharmacovigilance Associate (PVA) etc
What is the salary after a diploma in clinical research and Pharmacovigilance?
- The average salary After Completing this Course ranges from INR 2,50,000-INR 5,00,000.
Eligibility Criteria
- Minimum eligibility criteria for application to the courses are –
- MBBS
- B.Pharma
- BAMS
- BDS
- BHMS
- Physiotherapy
- Life sciences graduate
- Or with any of the following subjects botany, zoology, biochemistry, microbiology and biotechnology with min. 50%.
Curriculam
INTRODUCTION TO CLINICAL RESEARCH
BASIC TERMINOLOGY USED IN CLINICAL RESEARCH
INVESTIGATIONAL NEW DRUG
NEW DRUG DEVELOPMENT
CLINICAL TRIAL AND DESIGN
GUIDELINES FOR CLINICAL TRIALS (ICH-GCP)
ETHICS IN CLINICAL RESEARCH
REGULATIONS IN CLINICAL RESEARCH
CLINICAL TRIAL DOCUMENTS
QUALITY IN CLINICAL TRIALS
ROLES AND RESPONSIBILITIES IN CLINICAL RESEARCH
PARTICIPANT SAFETY & PHARMACOVIGILANCE