Qualified Person Education Course Module A - Online Training Recording

Qualified Person Education Course Module A - Online Training Recording

Kosten

ECA-Member*: EUR 1490,--
Regular Fee*: EUR 1690,--
EU/GMP Inspectorates*: EUR 845,--
QP Member Discount*: EUR 1490,--

Alle Preise zzgl. MwSt.

* auch unkompliziert per Kreditkarte bezahlbar American Express Visa Mastercard

Rückfragen unter:
Tel.: 06221 / 84 44 0 E-Mail: info@concept-heidelberg.de

Sprecher

Julia Gudd, GMP and GDP Inspector, Ministry of Justice and Consumer Protection, Hamburg, Germany
Dr Ulrich Kissel, European QP Association
Savvas Koulouridas, Fagron BV, The Netherlands
Aidan Madden FivePharma, Ireland
Sue Mann Sue Mann Consultancy, U.K.
Lance Smallshaw UCB, Belgium

Zielsetzung

Broaden and intensify your knowledge of the Qualified Person’s duties and responsibilities. Experts from the EQPA Board of Directors, pharmaceutical industry and regulatory authority will share their experience on important issues of the QP’s daily business and will give first-hand information on current and future expectations.

Hintergrund

Over the last years the roles and responsibilities of the Qualified Persons 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. This education course is one important part to help the QP be on top of current developments in GMP and regulatory requirements.

Zielgruppe

New and future Qualified Persons, QPs who are looking for ongoing training and personnel who want to get a detailed overview of the role and responsibilities of a QP.

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.

Programm

The Legal and Professional Duties of the Qualified Person
  • The Qualified Person within the EU legislation and regulation framework
  • Professional tasks, duties and responsibilities
  • Expectations of an EU GMP Inspector
Update on European Requirements
  • EU GMP Guide Chapters
  • EU GMP Guide Annexes
  • Other important News
  • What the QP needs to be aware of
Delegation of Duties and Responsibilities
  • Possible scenarios according to Annex 16
  • Mutual Recognition Agreements (MRA)
  • Documentation review issues
  • The QP in the quality system
Case Studies: Certification by a QP and Batch Release (to certify or not)
  • Batch certification: degrees of freedom and limits
  • Batch deviations and QP Certification
  • Examples: To certify or not, that’s the question
Case Study: Deviations during the Manufacture of an API – What Actions should you take as the responsible QP?
 
What the QP needs to know regarding the Supply Chain (from Supplier Qualification to GDP)
  • The QP: ultimate responsibility for the supply-chain of a drug product?
  • What is the expected scope of supply chain oversight
  • Supply chain integrity
  • Active Pharmaceutical Ingredient, Excipients, Bulk and Finished Product
  • Shipping under quarantine, ship to label claim, importation testing
  • The role of the QP in supplier qualification and auditing
  • Written confirmation and QP Declaration
  • GMP meets GDP: where does the responsibility end?
  • The QP’s involvement in the recall process
How the QP fits into the Quality Systems
  • How much involvement is needed in systems like:
  • Product Quality Review
  • Inspection Management
  • Batch Record Review
  • CAPA
  • Change Control
  • Validation
  • Complaints and recalls
Liability and Indemnification
  • Liability and indemnification of QPs
  • Role and responsibility of head of production and head of quality control (when things go wrong)
  • Role and responsibility of upper management (when things go wrong)
  • Delimitation of responsibilities with QPs in the same company
  • Delimitation of responsibilities with QPs at a contractor
What the QP needs to know about Pharmacopoeias
  • The world of different Pharmacopoeias
  • Pharmacopoeias are more than just Monographs
  • How to deal with different methods
Case Studies: What the QP needs to know about OOS/OOT
  • Involvement of the QP
  • Role and responsibility of the Head of Quality Control
  • Responsibility of the QP
Recording from 10/11 March 2022
Duration to the recording: about 11 h.

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