• Post category:StudyBullet-4
  • Reading time:4 mins read




PSMF and part of safety regular analysis

What you will learn

 

PSUR requirement, SOP process and how to develop, collect, reveiw & prepare the report for medicinal product

 

pharmacovigilance

 

PSUR SOP

 

PSUR Review

Description

PSUR is a regular document that get updated as per recent regulatory norms. It is needed for all the process related to safety surveillance and vigilance work. The PSUR have several component, it talks about the new safety information, emerging medical condition contraindicated, new information observed in the animal studies, information related to ongoing phase trials and planned post marketing surveillance studies. If a doctor and a literature report is found even this information is updated in the PSUR. Periodic report have measure of outcomes, daily dose use of the product, per day use and its impact, clinical trials , measures and its correlation with co morbid conditions. It allow authorities to take correct decisions, related to long term safety of the drug. In some case the faster approval path makes it difficult to understand the safety of the medication, or understand complete Benefit and risk ration of the drug. This presentation covers the PSUR requirement of the Guidelines of MAH for PMS safety. Chapter 3 explains the requirements and steps to be followed to prepare the report. The presentation is divided into the table of content, section of clinical trials data collection, reports of ongoing literature and safety studies, individual case reports and presentation in table format with division of source,gender and age groups.


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English
language

Content

Introduction

Introduction
General Introduction
PSUR Syllabus

PSUR Related Terminology

PSUR related Terminology
PSUR related Part 2 Terminology

PSUR India Related Regulatory

PSUR MAH India
Table of Content of PSUR

PSUR Check list

QC Process and Check list related to PSUR