Free DownloadWhat you'll 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 Requirements Basic Level of English Good quality of Internet connection Desktop, Laptop or Smartphone Description 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 RMPPrinciples of RMPResponsibilities of MAH in RMPFormat, Content and Template of RMPRMP parts and modulesCommon sections in RMP and PSURRisk minimization measures and Safety communicationsBy 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!!! Overview Section 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 Section 2: Format and Content of Risk Management Plan Lecture 5 Overview of the RMP Parts and Modules Lecture 6 RMP Part I - Product(s) overview Lecture 7 RMP Part II - Safety specification Lecture 8 RMP Part III - Pharmacovigilance plan Lecture 9 RMP Part IV: Plans for Post-authorisation Efficacy Studies Lecture 10 RMP Part V: Risk minimisation measures Lecture 11 RMP Part VI: Summary of the Risk Management Plan Lecture 12 RMP Part VII: Annexes to the Risk Management Plan Section 3: Risk minimization measures & Safety communications Lecture 13 Selection of tools, Effectiveness Indicators and aRMM Lecture 14 Effectiveness evaluation of risk minimisation measures Lecture 15 Safety communications Section 4: RMP template and other information Lecture 16 Template of RMP Lecture 17 Common Sections in RMP and PSUR Section 5: What to do after this training Lecture 18 What to do after this training 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)