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Industry Program In Clinical Research, Clinical Data Management & Pharmacovigilance - Gratisol Labs

Exploring Latest Trends in Pharmacovigilance and Clinical Trials in the era of COVID-19. Bringing Together Regulators, PV Professionals, Key Decision Makers And Solution Providers From The Global Pharma Industry Under One Roof For An Ultimate Knowledge Sharing And Networking Experience.

Industry Program In Clinical Research, Clinical Data Management & Pharmacovigilance

Advanced Certified Training Program in Clinical Research, Clinical Data Management & Pharmacovigilance

Pharmacovigilance is pharmacological science relating to detection, assessment and prevention of adverse effects of drugs. Improving drug safety is a task concerning not only regulatory authorities and pharmaceutical industry but also prescribing physicians. This is done right from the drug research and development stage to post marketing drug surveillance.

This course will provide extensive theoretical & training in Pharmacovigilance. All the topics will be presented by team of Doctors. It incorporates end-to-end theoretical & practical training on Pharmacovigilance processes including case assessment practical’s (seriousness of the events, reportablity of case, expectedness of the event) , Data Entry, Case Processing, Medical coding & Narrative Writing.

Following Course Content will be covered during the training:

  • Welcome and Introduction, History & Overview of Pharmacovigilance
  • Drug Development and Clinical Trial Phases
  • Introduction to Clinical Data Management
  • eCRF Design, UAT Testing, Discrepancy Management, Batch Validation
  • Pharmacovigilance Roles & Responsibilities in a CROs & Sponsor.
  • Pharmacovigilance Process & Life cycle
  • Introduction and responsibilities: USFDA, EMA and CDSCO
  • Pharmacovigilance in India
  • Clinical Development process
  • Different phases of clinical Trials
  • Adverse events and its types
  • Drug Safety in clinical trials and post marketed drugs
  • Different sources of Adverse events reporting
  • Different types of AE reporting Forms
  • Expedited reporting and its timelines
  • Different departments working on Pharmacovigilance
  • Roles and responsibilities of case receipt unit
  • Roles and responsibilities of Triage unit
  • Four factors for the reportable case
  • Seriousness criteria of adverse event
  • Expectedness or Listedness of adverse event
  • Causality assessment of the adverse event
  • Introduction to safety database and different types
  • Narrative writing
  • Case quality check, Medical review and its submission.
  • The Qualified Person for Pharmacovigilance (QPPV) in the European Economic Area
  • PSUR and its submission timelines

Minimum Eligibility Criteria For Application To The Course Would Be Either Of The Following:

Applicants are recommended to have one of the following life Science degrees: Bachelor’s, Master’s, or PhD, MBBS/ MD/B.D.S /M.D.S/ B.A.M.S / B.H.M.S /B.P.T/ B.Tech (Biotechnology / Pharmaceutical Science) / M.Tech (Biotechnology), B. Pharm /M.Pharm /BVSC / B.Sc. (Nursing) / B.Sc./M.Sc, M.Pharmacy, M.Sc /MA (Statistics) and all professionals working with Pharmaceutical companies, CROs and Hospital.

To Maintain High Academic Standard, Gratisol Labs Gives Due Importance To The Quality Of Students Enrolled. To Ensure This, The Selection Of Individual Student Will Undergo The Following Procedure:

Personal Interview

Screening And Selection Of Students


Complete Course Material will be provided including detailed information about the entire work flow of Drug Safety Associate.
2 months internship available after rigorous training in Pharmacovigilance.
Own CRO live Projects
We Provide Real Time Experience on Global Drug Safety Software with PSUR & DSUR Training.
Highest Placement record across all training institutes
Industry based SOP’s training
Trainers with minimum of 7+ years of experience
Comprehensive teaching by Medical Doctors
Hands on experience on Global Safety Databases used in the Industry.
Total 150 hours of exposure to theory, case studies and practicals.
Practical Hands on Training will be provided on Case Processing, Narrative Writing, MedDRA 16.1 & Who DRUG Coding


Resume Preparation
Interview Preparation with real time questions and answers
Mock Interview Sessions
Communication Skills and Personality development Sessions
Placement Assistance
Placement Assurance


Certificate will be provided for this Course on successful completion of Assignments & Projects. Certificate would be awarded at the end of the program by Gratisol Labs.

A fast track weekend course will also be conducted for employees & aspirants of Clinical Research Industry. For more information, please contact Gratisol Labs at training@gratisol.com.

  • 36
  • 60 hours
  • 2–5 hours per week
  • Gratisol Labs LLC
  • Clinical Data Management
  • Yes
  • English
  • English
  • Yes
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