Best Clinical Research Institute with all INDIA Branches

Pune's Only Government-Approved Clinical Research Institute

MITCON’s Clinical Research Department offers an ISO certified “Advanced PG Diploma in Clinical Research Course” to help you build an career in Clinical Research field.

Advanced PG Diploma in Clinical Research Course

Course Modules

1. Clinical Research Operations
2. Clinical Data Management (CDM)
3. Pharmacovigilance
4.Medical Writing
5. Regulatory Affairs
6. Interpersonal Skills

Course Eligibility

MBBS / BDS / BAMS, BHMS /B.PHARM, M. PHARM / B.Sc, M.Sc LIFE-SCIENCES, BIOTECH, NURSING graduates.

Job Opportunities

100 % Internship & Placement opportunities with over 500+ IT & Pharma Companies & over 200+ CRO's in clinical research field.

Why 'MITCON' is the best institute for Clinical Research in India ?

MITCON is India's only

institute supported by Department of Science & Technology (DST), Department of Scientific & Industrial Research ( DSIR), and MSME, Govt. of India.

Get hands-on experience with Practical’s

& Industry focused Software in Clinical Research Operations, Clinical Data Management, Pharmacovigilance, Medical Writing, Regulatory Affairs, and Interpersonal Skills to kick-start your dream career

Get Global Clinical Research

Certification with fully equiped Computer lab & one of the biggest Biotech lab with world class facilities.

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 focuses on mentoring through live projects and internships to solidify 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.

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..

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    Course Available all across India!

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