Comprehensive Program in Clinical Trials Data Management and Pharmacovigilance
Course
Online
*Indicative price
Original amount in RUR:
35,000
Description
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Type
Course
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Level
Advanced
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Methodology
Online
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Duration
6 Months
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Start date
Different dates available
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
Start date
About this course
• 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.
Final year post graduate Or graduate in any branch of Science with work experience in similar domain.
Reviews
Subjects
- Data Management
- Management
- IT Management
- Pharmacovigilance
- Biostatistics
- SAS
- CLINICAL TRIALS
- ICH
- GCP
- IRB
Teachers and trainers (1)
Dr Sachin Prajapati
Scientist
Course programme
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
Comprehensive Program in Clinical Trials Data Management and Pharmacovigilance
*Indicative price
Original amount in RUR:
35,000
