European GMPs and the Role of the Qualified Person (QP) (Day 1 and 2) + Clinical Trial Supplies (Day 3) – Online Training Recording

Course No. 20661A



Dr. Ulrich Kissel

Dr. Ulrich Kissel

European QP Association (EQPA), KisselPharmaConsulting

Dr. Rainer Gnibl

Dr. Rainer Gnibl

GMP Inspektor, Regierung von Oberbayern

Dr Susanne Ding

Dr Susanne Ding

Boehringer Ingelheim Pharma

All times mentioned are CEST.


This event is designed by QPs and international Experts as a forum with focus on sharing information and experience and on discussing the critical areas of European GMPs and the QP’s daily work.


The Pharmaceutical Industry has become more global due to international collaborations, mergers and acquisitions and more complex supply chains require companies to have a greater understanding of pharmaceutical legislation throughout the world. This is becoming increasingly evident by the number of non-EU professionals contacting the European Compliance Academy and the Qualified Persons Association asking for more and more detailed information about the European GMPs and the unique role and responsibility of the EU QP.

The ECA Academy and the European QP Association, recognising this need for further professional knowledge development, intend to support the pharmaceutical industry outside Europe in understanding the EU approach and legal framework in this respect. Therefore, the QP Association has set up the programme at hand on European GMP requirements and the role of the QP.

In light of the establishment of a Mutual Recognition Agreement between US and EU and the parallel move out of Great Britain from the EU, representatives from the authorities as well as QPs and well-known experts will talk about the current issues and share their point of view.

Target Group

The Conference has been designed for non-EU QA and QCU personnel, upper management functions and authority representatives who want to be informed about European GMPs and the duties and responsibilities of Qualified Persons.

Technical Details

To participate in an on demand training course or webinar, you do not need any software. The recordings are made available via a streaming server. In general, the recording is provided in MP4 format, which any PC (Microsoft Windows, Apple IOS) or tablet can easily display.
Timing and Duration: When you register for the on demand Training course or webinar you can decide at what date you want to follow the training course online. For a 1-day training course you will have 2 days in which the stream is available (for 2-day training course 3 days and for a 3-day training course 4 days). Within in this timeframe you can start & stop the stream according to your needs.
In time before the scheduled date (your desired date) you will receive an e-mail from us with a link for direct participation as well as your log-in data.
Training Course Documentation and Certificate:
The presentations will be made available as PDF files via download shortly before the online training course. After the event, you will automatically receive your certificate of participation.


Programme Part 1: Understand European GMPs | 11 – 12 July 2023

The EU Pharmaceutical Legislation and the respective Inspection System
  • EU legislation and relevant guidance documents (overview)
  • The EU inspection System
  • Non-compliance with EU-GMP and authority Actions
  • EU Manufacturing Authorisation & EU-GMP Certificate
  • MRA: impact for Industry
  • Exchange on GMP-information between US and EU
Export and Import of Medical Products
  • Annex 21 of the EU-GMP Guidelines
  • Import of Medicinal Products and APIs into the European Union
  • Which types of materials do fall under EU import legislation?
  • Regulatory requirements for Import
  • Which documents are needed for import activities of medicinal products and APIs
  • Regulatory procedure to get an import Licence
  • Procedure if a non-EU company imports to different EU Member States
The Role and Responsibilities of the QP
  • Batch certification and release for the EU Market
  • Directive 2001/83/EC; Article 49 – “conditions of qualification”
  • Annex 16 of the EU-GMP Guidelines
  • The role of the QP within the pharmaceutical quality System
  • What the QP is responsible for
  • The QP’s margin of discretion when certifying batches with deviations
  • Supply Chain oversight and supply chain diagram
  • QP Declaration
Distribution in the EU
  • GDP requirements
  • Importers, brokers, local affiliates, pre-wholesalers, wholesalers, parallel Import
  • Serialisation
  • Virtual companies
Brexit: Consequences for the pharmaceutical Industry
  • UK and EU Point of View
  • The Northern Ireland Protocol
  • Impact on the roles and responsibilities of the QP
  • What companies outside Europe need to be aware of
  • Examples of complications
When things go wrong
  • Complaint and recall handing
  • The QP and the QPPV
  • When to contact the authorities
Programme Part 2: Clinical Trial Supplies (optional) | 13 July 2023

Clinical Trial Supplies: IMP Handling in Europe and the Role of the QP
  • Current and future EU-GMP and QP requirements
  • Certification and release of Investigational Medicinal Products (IMPs) for studies in the EU
  • Specific aspects of IMP supply chains
  • GMP-GCP Interface
  • QP oversight and being a QP in a global environment
Question and Answer Sessions
When attending live online, a set of live Q&A Sessions will give you the possibility to interact with the Speakers and get answers to your questions.
Recording from 11-13 July 2023
Duration of Recording: approx. 10 h

ECA-Member*: € 1790,-
Regular Fee*: € 1990,-
EU/GMP Inspectorates*: € 995,-
QP Member Discount*: € 1790,-

(All prices excl. VAT). Important notes on sales tax.

* also payable by credit card
American Express Visa Mastercard

Further dates on-site
Further dates on-site
Not available
Further dates online
Further dates online
Not available

Do you have any questions?

Please contact us:
Tel.: +49 6221 8444-0

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