Comprehensive Program in Clinical Trials Data Management and Pharmacovigilance

Indian Biological Sciences and Research Institute
4.3
3 opinions
  • Good institute, quality courses, recommended for students.
    ← | →
  • The course is good and help in acquiring knowledge which help to get job and increase chance to select on the basis of course content.
    ← | →
  • Course content is good, easy to register, helpful in career.
    ← | →

Certificate

Distance

₹ 16,500 VAT incl.

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Description

  • Type

    Certificate

  • Methodology

    Distance learning

  • Duration

    12 Months

  • Start date

    Different dates available

  • Delivery of study materials

    Yes

  • Support service

    Yes

Certificate course is a skill development program designed to cover all aspects of Pharmacovigilance and drug safety management. It sensitizes the students and equips them with knowledge on Pharmacovigilance practices worldwide and on the Indian scenario in detail. This course gives young executives an opportunity to remain ahead of competitors in a very nascent yet competitive environment. The prime objective is to provide a high-end training thereby enhancing the employment prospects of the participants. Suitable for: MBBS/BDS/BAMS/BHMS/B PHARMACY/ BVSC/BSc LIFE-SCIENCE/ BIOTECH/M PHARMA/MSc/M Tech/ MD etc

Important information

Documents

  • ISO certification

Facilities

Location

Start date

Distance learning

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.

Final year post graduate Or graduate in any branch of Science with work experience in similar domain.

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

4.3
fantastic
  • Good institute, quality courses, recommended for students.
    ← | →
  • The course is good and help in acquiring knowledge which help to get job and increase chance to select on the basis of course content.
    ← | →
  • Course content is good, easy to register, helpful in career.
    ← | →
100%
4.3
fantastic

Course rating

Recommended

Centre rating

AMIT KUMAR TYAGI

5.0
10/03/2020
About the course: Good institute, quality courses, recommended for students.
Would you recommend this course?: Yes

AMIT KUMAR TYAGI

4.0
17/02/2020
About the course: The course is good and help in acquiring knowledge which help to get job and increase chance to select on the basis of course content.
Would you recommend this course?: Yes

Narendra Rathnakara

4.0
04/02/2020
About the course: Course content is good, easy to register, helpful in career.
Would you recommend this course?: Yes
*All reviews collected by Emagister & iAgora have been verified

Subjects

  • Pharmacovigilance
    2

    2 students say they acquired this skill

  • Data Management
    3

    3 students say they acquired this skill

  • Clinical trials
    3

    3 students say they acquired this skill

  • SAS
    1

    1 students say they acquired this skill

  • Biostatistics
    1

    1 students say they acquired this skill

  • Management
  • IT Management
  • GCP
    3

    3 students say they acquired this skill

  • ICH
    3

    3 students say they acquired this skill

  • IRB

Teachers and trainers (2)

Dr. Kumud Sarin

Dr. Kumud Sarin

Technical Head

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

₹ 16,500 VAT incl.

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