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Certification Verification

Enroll in Our Award-Winning Clinical Research Training – Advance Your Career Today!

One Program, Three Certifications!

CR, PV & CDM Training & Certifications

Now just 3999/- only

Duration: 3 Months

DIPLOMA IN CLINICAL RESEARCH

The Clinical Research industry continues to expand, with market projections reaching $165B by 2030 from $84B in 2025, showing a consistent CAGR. The PCCR certification provides comprehensive training in regulatory guidelines, research methodologies, and operational protocols, preparing professionals for various clinical research roles.

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DIPLOMA IN PHARMACOVIGILANCE

Pharmacovigilance focuses on monitoring drug safety through identification and prevention of adverse reactions. With growing global healthcare regulations, demand for trained professionals is rising. The Professional Certification in Pharmacovigilance (PCPhV) covers global standards, adverse event reporting, and evaluation procedures, preparing candidates for roles in pharmaceutical and healthcare sectors

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DIPLOMA IN CLINICA DATA MANAGEMENT

Clinical Data Management (CDM) coordinates clinical trials’ planning, monitoring, and success, focusing on schedules and milestones. The Professional Certification in Clinical Data Management (PCCDM) provides comprehensive training in data management strategies, CRF design, and database management, preparing candidates for roles like Data Coordinator, Manager, Reviewer, and QA Executive.

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SAMPLE CERTIFICATES

Program Overview

Clinical Research Excellence: Professional Online Training Program

Master the fundamentals of clinical research through our comprehensive live online training program. This industry-aligned curriculum prepares you for success in the rapidly growing healthcare research sector.

Core Specializations:

  • Clinical Research Fundamentals: Learn essential protocols, methodologies, and regulatory requirements that form the backbone of medical studies
  • Clinical Data Management: Develop expertise in handling, processing, and analyzing critical research data
  • Pharmacovigilance: Master drug safety monitoring and adverse event reporting systems

Program Details:

  • Duration: 4 months
  • Format: Flexible e-Learning
  • Full access to Learning Management System (LMS)
  • Interactive training video lecturers

Career Impact: Our program has a proven track record of success, with recent graduates securing positions at leading pharmaceutical companies, global Contract Research Organizations (CROs), and Fortune 500 healthcare firms. Whether you’re a life science student or professional looking to advance your career, this program provides the skills and knowledge needed to excel in clinical research.

Eligibility

Course level : Advanced
Duration : 4 Months
Examination Type : Module wise
Eligibility : Graduation in the Life Science (B.Sc/ M.Sc.), Pharmacy(B.Pharm/ M.Pharm), Nursing (B.Sc./M.Sc) Medical science courses (MBBS, BDS etc.)
Admission process : Evaluation Basis
Average salary : INR 2,50,000- INR 4,00,000 per year (Terms and Conditions applied)
Recruiting Organizations : Contract Research Organizations, 2. Information Technology Companies, Hospitals etc
Job Positions : CRA, CRC, DSA, Medical Writer etc