DIA会员及用户请点击登录

登录

忘记用户 ID? or 忘记密码?

Not a Member?

创建账户并加入。

Virtual Event

2023 年 02 月 21 日 9:00 上午 - 2023 年 02 月 24 日 1:30 下午

(Central Europe Standard Time)

4051 Basel, Switzerland

Pharmacovigilance Quality Management System

ONLY 2 SEATS LEFT! This beginner to intermediate level hands-on virtual live training course describes contemporary principles, practical approaches, and regulatory expectations for the Pharmacovigilance Quality Management System. NEXT COURSE TAKING PLACE 18-21 SEPTEMBER!

概览

This beginner to intermediate level virtual live training course will describe contemporary principles, practical approaches, and regulatory expectations for the Pharmacovigilance Quality Management System. The topics will cover organizational structure, responsibilities, processes and resources required for the pharmacovigilance (PV) system and its quality system. The course employs a mixture of informative instructional sessions, real-world case studies, and hands-on interactive exercises where attendees can apply what they learn. Learners will leave the course with an understanding of how elements of the Pharmacovigilance and Quality Management Systems fit together to achieve regulatory compliance.

A working knowledge of drug safety and pharmacovigilance principles is necessary in order to gain maximum benefit from the course.

 


What participants from the previous virtual QMS course say:

“This course was very great, I enjoyed it a lot! And I will implement some new ideas in my work.”
Ivonne Ramirez, PV Specialist, Boehringer-Ingelheim, Mexico

"Experienced Pharmacovigilance Consultant with a demonstrated history of working in the pharmaceutical industry. A high quality standard in relation to processes and data analysis. Able to act inter- and intradepartmental taken with the focus on teamwork. Acting EU-QPPV. Experienced in case processing, data analysis, EV reporting (ICSRs as well as art57/XEVMPD), compilation of pharmacovigilance system master files (PSMF), initial compilation and maintenance of CCDS and setting up PV systems. EMA and IGJ inspection experience. Eager to transfer knowledge to people in order to make them grow in the field of pharmacovigilance."
Bianca Schrans-Stassen, EU QPPV, Interdos, The Netherlands

"It was an excellent training, very well organised and brilliant tutors. Interactions with colleagues with experience in different areas of PV was an additional asset of the event. I would strongly recommend this training to all, but especially to people entering drug safety field."
Medical Information Pharmacist, UK


 

精选主题

  • What is a Quality System
  • How to set up a QMS
  • Exercise on listing the key/critical PV activities
  • Workshop on Gap Analysis of PV processes
  • Overview and description of the PSMF and PV Quality Manual
  • Risk Management Workshop
  • Process Flow Workshop
  • Safety Management Plans
  • Exercise on SDEA agreements
  • Commercial Activities and PV Obligations
  • Exercise on KPIs/metrics
  • Risk Assesment Worskhop
  • Record Management and Documentation of QMS
  • PV Inspections and Inspection Readiness
  • Inspection Findings Response Workshop
  • Root Cause Analysis Workshop

 

谁应该参加?

This course is designed for professionals involved in:

  • Quality assurance and compliance of the pharmacovigilance system 
  • Pharmacovigilance auditors 
  • Drug safety and pharmacovigilance personnel responsible for compliance, pharmacovigilance agreements, and/or pharmacovigilance quality documents
  • Pharmacovigilance activities at a pharmaceutical company or external service provider

Pharmacovigilance personnel who are considering the Pharmacovigilance Quality Management System field as a future career path would benefit from this course.

 

 

学习目标

At the conclusion of this course, participants will be able to:

  • Describe how to design, develop, and manage a quality system related to your pharmacovigilance system
  • Explain the components of the Pharmacovigilance Quality Manual 
  • Describe the process for the development and maintenance of the Pharmacovigilance System Master File
  • Analyze how the pharmacovigilance quality system integrates with the pharmacovigilance system 
  • Discuss the development, maintenance, and quality oversight of pharmacovigilance SOPs and pharmacovigilance related documents, including Safety Management Plans and PV Agreements across clinical study programs and post-marketing
  • Assess the effectiveness of the Quality Management System
  • Explain Quality Risk Management Planning for risk-based audits of the Pharmacovigilance System and Quality System
  • Define the scope of pharmacovigilance audits, including process audits, drug specific pharmacovigilance audits, and business partner pharmacovigilance audits
  • Describe how to prepare for audits and inspections
  • Practice preparing responses to a pharmacovigilance audit and inspection findings

 

Digital Learning Catalog

DIA Learning: eLearning Soultions
Download

获得信息并保持参与

不要错失任何机会——请加入我们的邮件列表,了解DIA的观点和事件。