Comprehensive Program in Clinical Trials Data Management and Pharmacovigilance

Indian Biological Sciences and Research Institute

Course

Online

₹ 35,000 VAT incl.

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Description

  • Type

    Course

  • Level

    Advanced

  • Methodology

    Online

  • Duration

    6 Months

  • Start date

    Different dates available

  • Delivery of study materials

    Yes

  • Support service

    Yes

  • Virtual classes

    Yes

This is the Comprehensive Program in Clinical Trials Data Management and Pharmacovigilance Certificate course endorsed by Indian Biological-science and Research Institute and offered on Emagister.

Facilities

Location

Start date

Online

Start date

Different dates availableEnrolment now open

About this course

Course intended for keen interested students and professionals who want to enter and grow in this field.

Science graduate with similar work experience OR science post graduate Or working professionals in similar domain.

Candidates with MBBS / B.D.S / B.A.M.S / B.H.M.S /B. Pharmacy / BVSC/ B.Sc. (Nursing)/ M.Pharma are eligible. Educational qualification and experience in the field of medical sciences, life sciences, data management, and clinical research. Even B,Sc life sciences or B.Tech in Biotech are eligible for the course.

This program is under flagship program of the institute and industry demanding program.

On receiving your request for the program, our team member will contact you and assist you if you have any related query.

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Reviews

Subjects

  • Management
  • Data Management
  • IT Management
  • Pharmacovigilance
  • SAS
  • Clinical Trial
  • ICH
  • GCP
  • IRB
  • Biostatistics

Teachers and trainers (1)

Dr. Sachin Prajapati

Dr. Sachin Prajapati

Scientist-Clinical Research and Pharmacovigilance

Course programme

These are the papers covered in this course-

Paper-I: Introduction to Clinical Trials
Paper-II: Introduction to Clinical Trials Data Management
Paper-III: Principles of Pharmacovigilance
Paper-IV: Biostatistics, SAS and Data Management
Paper-V: Computerized Systems for E- Case Report Form and Data Acquisition and Validation
Paper-VI: Methodologies in Pharmacovigilance and Signal Detection
Paper-VII: GCP, ICH, Ethics, IRB, Regulations for Clinical Trials
Paper-VIII: Pharmacovigilance Compliance and Management
Paper-IX: Case Study Report

See related categories

Comprehensive Program in Clinical Trials Data Management and Pharmacovigilance

₹ 35,000 VAT incl.

The best Pharmacy and Clinical Research courses

See all

See all