Best Clinical Research Institute with all INDIA Branches

Join the Clinical Research Revolution with MITCON's Clinical Research Institutes all over India.

☞ Become an expert in Clinical Research with the Advanced PG Diploma in Clinical Research Course offered by MITCON Clinical Research Department.

☞ Get hands-on experience in Clinical Research Operations, Clinical Data Management, Pharmacovigilance, Medical Writing, Regulatory Affairs, and Interpersonal Skills to kickstart your dream career.

☞ Our institute is ISO certified and SIRO recognized by DSIR technology, and is funded by the Department of Science.

Our Vision

Investing in your future, we provide innovative and impactful education to empower the industry leaders of tomorrow.

Our Mission

Our mission is to provide you with the most relevant and practical knowledge in all areas of Clinical Research, creating the best foundation for a successful career.

Our Process

We take a tailored approach with every student, working closely towards personal and professional growth while mentoring through live projects and internships solidifying theoretical knowledge into practical skills.

Our Team

Our esteemed faculty feature national and international experts in the field, spanning multiple specialties and providing unparalleled guidance.

Enroll now in a location near you.

Advanced PG Diploma in Clinical Research Course

Course Modules

Our comprehensive course includes Clinical Research Operations, Clinical Data Management (CDM), Pharmacovigilance, Medical Writing, Regulatory Affairs and Interpersonal Skills

Course Eligibility

The Advanced PG Diploma course in clinical research can be enrolled by MBBS / BDS / BAMS, BHMS /B.PHARM, M. PHARM / B.Sc, M.Sc LIFE-SCIENCES, BIOTECH, NURSING graduates.

Job Opportunities

Joining our advanced post graduate diploma in clinical research course opens up a plethora of job options with over 12+ career choices & job opportunities in clinical research field.

Course Available all across India!

choose your location

Course

content

Clinical Research Operations

Module 1

  • ICH-GCP Guidelines
  • New Drug & Clinical Trials Rules
  • TMF/eTMF

Clinical Data Management (CDM)

Module 2

  • Introduction to CDM & Process flow of CDM
  • Data entry & Database
  • Data review & Essential documents in CDM

Pharmacovigilance

Module 3

  • Introduction to Pharmacovigilance
  • Eudravigilance & Signal Detection
  • PSUR & CIOMS/MedWatch

Medical Writing

Module 4

  • Introduction to Medical Writing & Protocol Writing
  • IB & ICD Writing
  • Manuscript & Publication Writing

Regulatory Affairs

Module 5

  • Regulatory Agencies
  • Common Technical Documents – CTD (API & Formulation)
  • Introduction to eCTD

Interpersonal Skills

Module 6

  • Soft Skill Development & Presentation Skills
  • CV Preparation / Writing
  • LinkedIn Profile Creation & Networking

strong alumni network

3000+ Students Trained.
Now it's your turn..