🎓 Integrated Clinical Research, Pharmacovigilance & Drug Regulatory Affairs Internship

With Project Report, Thesis & Industry Exposure (Online Mode)

🚀 Program Overview

Step into the pharmaceutical and clinical research industry with our industry-oriented online internship program designed for Final Year Students & Pass-outs in Life Sciences, Pharmacy, and Biotechnology.

This internship combines Clinical Research, Pharmacovigilance (Drug Safety), and Drug Regulatory Affairs into one powerful learning experience—enhanced with real-world case studies, project work, and a structured thesis report.

📅 Key Highlights

• ✅ Mode: 100% Online (Live + Recorded Sessions)
• ✅ Duration Options:
  • 2 Months (Fast Track)
  • 3 Months (Advanced + Thesis Focus)
• ✅ Classes: 2 Sessions per Week
• ✅ Live Practical Exposure + Case Studies
• ✅ Project + Thesis Included
• ✅ Industry-Oriented Curriculum

🎯 Who Should Enroll?

• Final Year Students (B.Pharm, M.Pharm, BSc, MSc, Biotech, Life Sciences)
• Freshers / Pass-out Students
• Candidates looking for careers in:
  • Clinical Research
  • Pharmacovigilance
  • Drug Regulatory Affairs

📘 What You Will Learn

🔬 Clinical Research

• Clinical Trial Phases & Design
• ICH-GCP Guidelines
• Informed Consent Process
• Case Report Forms (CRF)
• Roles in Clinical Trials

💊 Pharmacovigilance (Drug Safety)

• Adverse Drug Reaction (ADR) Reporting
• ICSR & Narrative Writing
• MedDRA Coding Basics
• Signal Detection Concepts
• PSUR & Safety Reporting

📑 Drug Regulatory Affairs

• Global Regulatory Bodies (CDSCO, USFDA, EMA)
• CTD & eCTD Structure
• IND, NDA, ANDA Overview
• Drug Approval Process
• Labeling & Compliance

📊 Internship Project & Thesis

📌 Project Title

“Evaluation of Drug Safety and Regulatory Compliance in Clinical Trials: A Pharmacovigilance Perspective”

🧪 Project Work Includes

• Clinical Trial Case Study Analysis
• ADR Case Processing & Reporting
• Mock Regulatory Documentation
• Safety Data Interpretation

📄 Thesis Report (Portfolio Ready)

• Structured Research-Based Report
• Literature Review + Data Analysis
• Industry-Relevant Format
• Guidance & Mentorship Provided

🛠️ Tools & Practical Exposure

• ADR Form Filling Practice
• Case Study Discussions
• Mock Regulatory Submission Files
• Real Industry Documentation Understanding

🎓 Certification & Deliverables

• Internship Completion Certificate
• Project Completion Certificate
• Thesis Report (Ready for Submission/Portfolio)
• Case Study Portfolio
• Letter of Recommendation (based on performance)

📈 Learning Outcome

After completion, you will be able to:

• Understand Clinical Trial Processes
• Perform Basic Pharmacovigilance Activities
• Interpret Drug Safety Data
• Understand Regulatory Documentation
• Build a Strong Job-Ready Profile

🧑‍🏫 Additional Benefits

• Resume Building Session
• LinkedIn Profile Optimization
• Mock Interviews
• Industry Expert Sessions

📅 Batch Details

• New Batch Starts: 15th May 2026
• Last Date to Enrol: 30th April
• Limited Seats Available

💼 Career Opportunities After Completion

• Clinical Research Coordinator (CRC)
• Pharmacovigilance Associate
• Drug Safety Associate
• Regulatory Affairs Executive
• Clinical Data Associate

📢 Enroll Now

Kickstart your career in the pharmaceutical and clinical research industry with hands-on experience and industry exposure.

👉 Contact LearnToUpgrade Team for Enrollment Process