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
Speakers
Dr Ulrich Kissel
European QP Association (EQPA), KisselPharmaConsulting
Dr Rainer Gnibl
GMP Inspector
David Cockburn
form. European Medicines Agency (EMA)
Dr Susanne Ding
Boehringer Ingelheim Pharma
All times mentioned are CEST.
Objectives
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.
Background
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
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.
Testimonials