Pharmacovigilance Risk Management Plan: Step by Step Guide

Pharmacovigilance Risk Management Plan: Step by Step Guide, available at $59.99, has an average rating of 3.45, with 18 lectures, based on 41 reviews, and has 266 subscribers.

You will learn about Introduction and Objectives of RMP Terminologies in RMP Principles of RMP Responsibilities of MAH in RMP Format, Content and Template of the RMP Common sections in RMP and PSUR Template of RMP Risk minimization measures & Safety communications This course is ideal for individuals who are Pharmacovigilance Experienced candidates or Graduate or Postgraduate degree in Pharmacy (e.g., B Pharm, M Pharm, M S Pharm, Pharm D) or Graduate or Postgraduate degree in Medicine (MBBS, MD, BAMS, BUMS, BHMS) or Graduate or Postgraduate degree in Life Sciences (BSc, MSc, PhD) It is particularly useful for Pharmacovigilance Experienced candidates or Graduate or Postgraduate degree in Pharmacy (e.g., B Pharm, M Pharm, M S Pharm, Pharm D) or Graduate or Postgraduate degree in Medicine (MBBS, MD, BAMS, BUMS, BHMS) or Graduate or Postgraduate degree in Life Sciences (BSc, MSc, PhD).

Enroll now: Pharmacovigilance Risk Management Plan: Step by Step Guide

Summary

Title: Pharmacovigilance Risk Management Plan: Step by Step Guide

Price: $59.99

Average Rating: 3.45

Number of Lectures: 18

Number of Published Lectures: 18

Number of Curriculum Items: 18

Number of Published Curriculum Objects: 18

Original Price: ₹1,799

Quality Status: approved

Status: Live

What You Will Learn

Introduction and Objectives of RMP
Terminologies in RMP
Principles of RMP
Responsibilities of MAH in RMP
Format, Content and Template of the RMP
Common sections in RMP and PSUR
Template of RMP
Risk minimization measures & Safety communications

Who Should Attend

Pharmacovigilance Experienced candidates
Graduate or Postgraduate degree in Pharmacy (e.g., B Pharm, M Pharm, M S Pharm, Pharm D)
Graduate or Postgraduate degree in Medicine (MBBS, MD, BAMS, BUMS, BHMS)
Graduate or Postgraduate degree in Life Sciences (BSc, MSc, PhD)

Target Audiences

Pharmacovigilance Experienced candidates
Graduate or Postgraduate degree in Pharmacy (e.g., B Pharm, M Pharm, M S Pharm, Pharm D)
Graduate or Postgraduate degree in Medicine (MBBS, MD, BAMS, BUMS, BHMS)
Graduate or Postgraduate degree in Life Sciences (BSc, MSc, PhD)

This course is exclusively designed for Pharma students, Medical practitioners and Life science graduates.

This course will be helpful to those who have ICSR, Aggregate Reporting or Signal management experience in Pharmacovigilance domain and for those who wants to learn and excel their career in Pharmacovigilance Risk Management Plan (RMP).

This Job role (Risk Management Expert) comes under Niche Skill, which means there is high demand and less resources available in the industry. This is one of the high paying Job Role in Pharmacovigilance/ Pharma domain.

The Trainer of this course has more than 11 years of Pharmacovigilance Industry Experience from different multinational companies (MNC). He has expertise in ICSR, Aggregate Reports, Signal and Risk Management.

In this course we have covered following topics:

Introduction and Objectives of RMP
Principles of RMP
Responsibilities of MAH in RMP
Format, Content and Template of RMP
RMP parts and modules
Common sections in RMP and PSUR
Risk minimization measures and Safety communications

By completing this course, you will be more confident to face your interview in Pharmacovigilance Risk Management. You will learn new aspects of pharmacovigilance Risk Management.

We hope you will find this course very helpful, and you will land your dream job in Pharmacovigilance Risk Management very soon.

Good Luck!!!

Course Curriculum

Chapter 1: Basics of Risk Management Plan (RMP)

Lecture 1: Introduction and Objectives of RMP

Lecture 2: Terminologies in RMP

Lecture 3: Principles of RMP

Lecture 4: Responsibilities of MAH in RMP

Chapter 2: Format and Content of Risk Management Plan

Lecture 1: Overview of the RMP Parts and Modules

Lecture 2: RMP Part I – Product(s) overview

Lecture 3: RMP Part II – Safety specification

Lecture 4: RMP Part III – Pharmacovigilance plan

Lecture 5: RMP Part IV: Plans for Post-authorisation Efficacy Studies

Lecture 6: RMP Part V: Risk minimisation measures

Lecture 7: RMP Part VI: Summary of the Risk Management Plan

Lecture 8: RMP Part VII: Annexes to the Risk Management Plan

Chapter 3: Risk minimization measures & Safety communications

Lecture 1: Selection of tools, Effectiveness Indicators and aRMM

Lecture 2: Effectiveness evaluation of risk minimisation measures

Lecture 3: Safety communications

Chapter 4: RMP template and other information

Lecture 1: Template of RMP

Lecture 2: Common Sections in RMP and PSUR

Chapter 5: What to do after this training

Lecture 1: What to do after this training

Instructors

PV Drug Safety Academy
Pharmacovigilance Consultant| Pharmacovigilance Trainer

Rating Distribution

1 stars: 3 votes
2 stars: 2 votes
3 stars: 15 votes
4 stars: 11 votes
5 stars: 10 votes

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