Georg Göstl
Takeda Manufacturing Austria
Referent:innen
Dr Ulrich Kissel
European QP Association (EQPA), KisselPharmaConsulting
Dr. Jens-Uwe Rengers
vorm. Akorn
Ewa Rybak
Polpharma Biologics
Zielsetzung
Broaden your knowledge of the Qualified Person’s duties and see and discuss which responsibilities and tasks are parts of a QP’s daily life – besides batch certification. With fulfilling these tasks, the QP has a lot of interfaces and interactions. How this can be managed will be a topic in Module B and its pre-course session on soft skills.
Hintergrund
Over the last years the role and responsibilities of the Qualified Person have been increasing considerably. As a key person in the company, the QP has to consider many issues and has to take up the challenges within its areas of responsibilities. Additionally, as laid out in Article 49 of the European Directive 2001/83/EC, the QP needs to be highly qualified and experienced. EQPA’s education course modules will help the QP to be well prepared and to be on top of current developments in GMP and regulatory requirements.
Zielgruppe
New and practicing Qualified Persons who are looking for ongoing training and want to improve their effectiveness and liaison with other functions.
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.
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.
Programm
QP Interfaces
- Which roles are essential for a QP to work efficiently and effectively (e.g. Head of Production, Head of Quality Control, QPPV, QA)
- Identifying the best working practice for QPs working with colleagues in supportive roles
- Links with regulatory authorities and inspectors
Import – Export – Product Flow
- Applicable legislation: a view on Annex 16 and Annex 21
- Different Mutual Recognition Agreements (MRAs)
- What’s expected with regard to Supplier Qualification, Supply Chain Overview, Re-Testing and PQ
Interpretation of Data (with a Focus on Batch Documentation and the PQR)
- Which key figures are relevant for the QP?
- Data verification: determining the acceptability of data
- When is a system or process deemed to be robust?
- Necessary key figures: always easy to understand?
- When is a trend a trend? And what to do with OOT (out of trend)?
Interpretation of Data
- Learn how to interpret data and understand the consequences of appropriate and inappropriate performance parameters
- Evaluate with other delegates the content and lay-out of given examples and discuss it with the speakers
Human Error
- What is behind “Human Error”?
- What the QP needs to know about it
- Is Human error avoidable?
- Human error and Data Integrity issues
How to ensure that a Batch is in Compliance with the Requirements of its Marketing Authorisation (MA)
- Structure of the MA – which are the relevant parts for the QP?
- How to keep the QP Declaration up to date?
- How can the QP ensure compliance?
- Involvement in Change Control processes
- Challenges for the QP
- Possible Work Flows
Quality Risk Management for the QP
The term “quality risk management” is used throughout Annex 16. But how could the QP use this tool? In this session you will get some practical advice!
The term “quality risk management” is used throughout Annex 16. But how could the QP use this tool? In this session you will get some practical advice!
QP Involvement in Investigations and CAPA
- QP role in deviation process
- Product Deviation
- Process deviation
- Reoccurring deviations - QP role in handling of product deviations
- Does QP need to be involved in all deviations?
- QP final decision regarding product deviation and batch certification
- QP involvement in product complaints
- Tools for performing investigations
- The importance of CAPA in the deviation process
- Workshop with examples
Thinking outside the Box: Certification of Plasma Products
New classes of medicines such as ATMPs, Blood and Plasma Products are creating special challenges for the QPs certifying
these products. This session aims to provide insight into the challenges when certifying plasma products. Discuss these challenges and see what delegates from different areas can learn from each other.
New classes of medicines such as ATMPs, Blood and Plasma Products are creating special challenges for the QPs certifying
these products. This session aims to provide insight into the challenges when certifying plasma products. Discuss these challenges and see what delegates from different areas can learn from each other.
Recording from 30.06.-01.07.2021
Duation of the recording: approx. 12 hours
Duation of the recording: approx. 12 hours
| ECA-Member*: | € 1490,- |
| Regular Fee*: | € 1690,- |
| EU/GMP Inspectorates*: | € 845,- |
| QP Member Discount*: | € 1490,- |
Alle Preise zzgl. MwSt. Wichtige Hinweise zur Umsatzsteuer.
* auch unkompliziert per Kreditkarte bezahlbar
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