About
A robust Quality Management System (QMS) is the backbone of pharmacovigilance, ensuring that the safety profile of medicines is rigorously monitored and maintained.
This course introduces participants to the QMS required in pharmacovigilance.
The objectives of the training are to explore the QMS framework, the different types of audits and their required procedures and management, to consider corrective and preventive actions and to gain insight into the effective management of audit findings.
The programme will also cover important aspects such as training components, maintenance of training records and retention of pharmacovigilance documents. It will also highlight various metrics that are critical to monitoring process compliance and fostering a culture of continuous improvement.
Quality Management System: The Structure
Audit Programme
- Inbound and Outbound
- Setting up an Audit Universe
- Developing an Annual Audit Programme
- Audit Strategy
- Tactical and Operational Planning
- CAPA Management
PV Training
- Internal & external training
- Regulatory training
- Continuous development
Records Management
- PV document retention
- Training records
- Facilities
- Destruction process
Compliance and metrics
- Develop and monitor metrics
The course is aimed at pharmacovigilance professionals responsible for quality management activities and metrics, as well as QA professionals will to become an auditor.
Participant experience
Basic Pharmacovigilance experience is required
Interactive training; presentation and workshop exercises
Lecturers
Ranjana Khanna
Ranjana has a Masters in Technology and a Post Graduate DIploma in Pharmacovigilance. She has been working in this field since 2004, starting her career in Safety Case Processing in a CRO followed by working in various Pharmaceutical companies. Since 2012, Ranjana has been responsible for Pharmacovigilance Quality assurance which includes conducting all types of audits, leading HA Inspections, providing Training and overseeing all QMS aspects. She has led teams globally, presented at several conferences and published articles on aspects of Pharmacovigilance QA.
Online Training – 2 modules
MODULE 1 | 19 November 2024 from 9:00 am to 1:00 pm CET
MODULE 2 | 21 November 2024 from 9:00 am to 1:00 pm CET
After the registration, you will receive all details about the connection.
The course will proceed with a minimum number of participants. Should this number not be reached the registered participants will be notified one week prior to the commencement of the course.
Early Bird: € 895,00* (until 05 November 2024)
Ordinary: € 1.095,00*
Freelance – Individual – Academy – Public Administration: € 640,00*
* for Italian companies: +22% VAT
The fee includes: tuitions, organizational office assistance, teaching materials and attendance certificate that will be sent after the training via e-mail.
Register
Ilaria Butta
Events & Training Manager
At the end of the training, you will be able to
Online interactive training on Zoom platform.
LS Academy will provide the access link to the virtual platform a few days before the training.