David Abraham
QRS-Associates
Referent:innen
Dr Daniel Müller
GMP Inspector
Alfred Hunt
Hunt Pharma Solutions
Heike Gottschalg
Boehringer Ingelheim Corporate Center
Robert Müller
Boehringer Ingelheim
Savvas Koulouridas
Fagron BV
Zielsetzung
This Live Online Training provides practical guidance to bring and keep your organisation in compliance with the GDP regulations.
Hintergrund
The globalisation of the pharmaceutical supply chain has created new challenges for the manufacture and supply of medicinal products in various markets, resulting in reduced control and increased security risk to the products.
The EU-GDP Guidelines have been extensively revised to take into account the changing nature of the globalised supply chain. The requirements have been effective since 2013. These requirements highlight the need for an effective quality management system supported by risk assessment and appropriate controls.
This two-day Live Online Training has been designed to bring you up-to-date with the current regulatory expectations and standards for Good Distribution Practice (GDP) and to provide you with tools and guidance to help you with identifying the gaps in your quality systems and planning and implementing the actions required.
The EU-GDP Guidelines have been extensively revised to take into account the changing nature of the globalised supply chain. The requirements have been effective since 2013. These requirements highlight the need for an effective quality management system supported by risk assessment and appropriate controls.
This two-day Live Online Training has been designed to bring you up-to-date with the current regulatory expectations and standards for Good Distribution Practice (GDP) and to provide you with tools and guidance to help you with identifying the gaps in your quality systems and planning and implementing the actions required.
Zielgruppe
GDP Compliance Managers and Responsible Persons from companies involved in the distribution and supply of medicinal products.
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.
Please be aware: The recording does not include the Q & A sessions.
Training Course Documentation and Certificate:
The presentation will be made available as PDF-files via download during the online training course. After the successful completion of the online training, you are able to download the certificate of attendance.
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.
Please be aware: The recording does not include the Q & A sessions.
Training Course Documentation and Certificate:
The presentation will be made available as PDF-files via download during the online training course. After the successful completion of the online training, you are able to download the certificate of attendance.
Programm
Welcome and Introduction
The (new) GDP Guideline: What was it all about?
- Background to development and revision of the EU GDP Guidelines
- Overview of structure and Content
- What is the impact on industry and other stakeholders?
Quality Management System (QMS)
- What is a QMS and why do we need it?
- What does an effective QMS look like?
- How to develop and implement an effective QMS Operations
- Qualification of suppliers and customers
- Receipt, storage and return of medicinal products
- Deviation and Complaint Management in a wholesaler facility
- How to conduct a gap analysis, develop plans and implement the new requirements
GDP Inspection Findings and what to learn from them
- Findings and their Ratings
- Examples from manufacturers, wholesalers, storage facilities and transport deviations
Personnel
- Competency requirements for GDP personnel
- Overview of the role and responsibilities of the Responsible Person
- Necessary documentation
- Training matrix and managing continuous training
Premises & Equipment
- What is a must for medicinal products
- How to plan and implement facility improvement ensuring compliance with the current requirements
Transportation
- Key requirements for transportation of medicines
- How to develop and implement a GDP-compliant and cost effective transportation network.
Contracts in the Global Supply Chain
- International laws and systems – how they work and fit together
- Jurisdictions and conflict of law provisions
- Contract law, Technical/ Quality Agreement, Supply Agreement
- 3PL Providers: two bilateral agreements or one tripartite agreement?
- When things go wrong
Outsourced Activities
- What is an outsourced activity?
- How to set priorities to audit, approve and manage Service Providers
- How to develop and manage contracts and agreements
Case Study for a successful Implementation Approach
- How we approached the new requirements
- Challenges and best practice
Short Summary and Take Away Message
- Developing a take home action plan for the delegates
Recording from 19/20.11.2024
Duration of the recording: approx. 10 hours
Duration of the recording: approx. 10 hours
| ECA-Member*: | € 1690,- |
| Regular Fee*: | € 1890,- |
| EU/GMP Inspectorates*: | € 945,- |
| APIC Member Discount*: | € 1790,- |
| GDP Association Member Discount*: | € 1690,- |
Alle Preise zzgl. MwSt. Wichtige Hinweise zur Umsatzsteuer.
* auch unkompliziert per Kreditkarte bezahlbar
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