Pharmacovigilance Officer In Charge in India

It help to understand the types of responsibilities of a officer taking up the role
English
English [Auto]
Indian Pharmacovigilance Officer in charge selection role and responsibilities are described in the MAH guidelines, this program help you to understand complete activity of the global pharmacovigilance officer role and functioning in India. This cover many section and activities that this PVIO should be carrying out in the pharma company

Requirements

  • Pharmacovigilance officer in charge can be a medical qualified person, or a master in pharmacology or a pharma D qualified person, or a dentistWorking in health care sector, should be working in pharmaceutical firm or h

Description

Pharmacovigilance officer in-charge is  major role in India. When you are taking up a a job or attending a interview it is important to know about the role. Company starting pharma production can also use this presentation to understand the multiple implications. The role involves monitoring multiple location, tracking of incoming reports, hands on experience in setting up of operational procedures, creation of training timing, creation of audit schedules,management of report and signal detections

Who this course is for:

  • pharmaceutical firms need to have a pharmacovigilance officer in charge in place as per recent changes in regulatory authorties. Hence the company top management, department of quality assurance and audits, and manpower hiring team should know the knowledge requirements and functions of this role.

Course content

5 sections5 lectures1h 53m total length
  • Introduction
    19:05

Instructor

PSMF, Auditor
Dr.Banu Priya
  • 4.1 Instructor Rating
  • 29 Reviews
  • 945 Students
  • 1 Course

Ph.D in Toxicology, designed PSMF software's for Indian Pharma firms as per MAH Guidelines, android solutions and automatic audit systems for pharmaceutical firms. Have created SOP for pharmacovigilance process, created audit procedures, ADR reporting, processing, data collection and review, created training material for all modules of MAH guidelines for Indian PSMF file management. Have work experience of 20 years  in senior management, clinical research, audit and data management. have conducted several senior management pharmacovigilance review and risk management plans for various products.