Training Overview

Under European post-marketing drug legislation it is a legal requirement to have a document produced – the Pharmacovigilance Systems Master File (PSMF).

This document covers the pharmacovigilance for all licensed products in the EU as well as any licences outside of the EU for the same product.

The document therefore covers pharmacovigilance that is global and not just confined to the EU.

This document covers activities related to pharmacovigilance which include Regulatory; Clinical; IT; QA and the Marketing Dept.

This document has also to be inspection ready and following the announcement of a Regulatory Inspection is the first document requested.

 Webinar Includes : All the training handouts , certificate ,Q/A and 90 mins Live Webinar

Why Should You Attend

People should attend this training:

  • To understand the requirement of producing the PSMF and its maintenance
  • The requirement to have this as an inspection ready document
  • The understanding of CAPA inclusions and removals 
  • The oversight of the PSMF and the involvement of the EU QP PV

Webinar Takeaway

  • The evolution of the PSMF and the legislation concerning it for the EU
  • Other PSMFs globally and linkage to other PSMFs
  • The sections of the PSMF
  • The annexes of the PSMF
  • Audits and the PSMF including CAPAs
  • Multiple Depts and their involvement with the PSMF
  • Regulatory Inspections and the PSMF

Key Learning Objectives

  • To understand the key elements of the main body of the PSMF
  • Management of the Annexes with the PSMF
  • Frequency of PSMF review
  • Other PSMFs globally
  • Review and approval of the PSMF

Who Will Benefit

The various Depts that will benefit from this training are:

  • Pharmacovigilance
  • Newly appointed EU QP PVs
  • Global Heads of PV
  • Regulatory
  • Clinical
  • IT
  • Sales & Marketing
Graeme Ladds

Graeme Ladds

CEO PharSafer Associates Ltd - Global Leaders in Drug Safety

England, United Kingdom

With a first degree in Biochemistry & Pharmacology and a PhD focussing on drug metabolism and Pharmacokinetics Graeme has worked in the areas of Drug Safety and Medical services for nearly the last 30 years.

Graeme has been working as Head of Global Pharmacovigilance and EU QP PV for many large (and small) Pharma, and has been CEO for the last 17 years for PharSafer.

Graeme is also a member of TOPRA; RQA and the Institute of Directors and has helped small start up Companies in their planning, growth and been involved in Company acquisitions, due diligence activities for product in-licensing and marketing and development strategies.

Choose a Purchase Option


$299

Recorded Access Corporate Group

You'll have 12 month access to group log-in for an archived recording of the entire 90-minute webinar, including the Q&A period. You can log in any time of day or night. You'll also receive all presentation materials, plus an audio recording and transcript for the entire session. Delivery is approximately 48 hours after the session

$399

MP3 Download - Training DVD

Within 48 hours delivered - Lifetime Access ,Audio recording of a webinar and reference manual delivered by download. Listen anytime on any compatible device.

Our Participants Testimonial


The presentation by Carolyn Troiana today was fantastic, both I and the QA Manager (Aaron Neighbour) loved it and had extensive conversation afterward about it. ( FDA Compliance and Mobile Applications Webinar )

Robert Friedland ( IT Manager) NUTEK BRAVO, LLC.

Thank you for providing the information in such detail. It was helpful to gain the perspective of somebody that has implemented these regulations in a working lab. Virtual Seminar on ( Training on Life cycle Management of Analytical Methods and Procedures - according to new FDA and USP guidelines )

Tracey Kessler ( Director of R&D) CEL-SCI Corporation

I felt the seminar was very helpful and provided good insight for DataIntegrity and what the FDA is looking for per the regulations. ( Current Regulatory Thinking on Data Integrity 2 Days Virtual Seminar )

Margaret A. Clifton ( Manager, Quality Systems) CSL Plasma

The presenters subject matter knowledge is extensive which enables information to be shared in detail. (Training Attended on Risk Based Verification and Validation Planning to Meed US FDA and ISO 13485 Requirements )

Stuart Chisholm (Sr. Principal Device Engineer) Teva Pharmaceuticals