Dr Torsten Schmidt-Bader
moveproTEC Compliance & Innovation Advisory
Referent:innen
All times mentioned are CET.
Hintergrund
The storage and transport of medicinal products are subject to strict regulatory requirements. Good Distribution Practice (GDP) is a crucial component of pharmaceutical quality management, ensuring that product quality is maintained throughout every stage of the supply chain. With increasing regulatory demands and the continued globalization of distribution networks, documented compliance with GDP guidelines is more important than ever.
Many logistics activities within the supply chain are outsourced to service providers, such as transport and logistics companies. While companies that only perform transportation activities are not subject to direct regulatory oversight and do not require a Wholesale Distribution Authorisation (WDA), they are still expected to comply with the relevant sections of the EU GDP Guidelines.
For logistics service providers, external GDP certification can be a valuable tool to demonstrate compliance and commitment to quality standards. Commercial certifications offer a structured approach – but their reliability and practical relevance are increasingly being questioned.
Many logistics activities within the supply chain are outsourced to service providers, such as transport and logistics companies. While companies that only perform transportation activities are not subject to direct regulatory oversight and do not require a Wholesale Distribution Authorisation (WDA), they are still expected to comply with the relevant sections of the EU GDP Guidelines.
For logistics service providers, external GDP certification can be a valuable tool to demonstrate compliance and commitment to quality standards. Commercial certifications offer a structured approach – but their reliability and practical relevance are increasingly being questioned.
Zielgruppe
This webinar is aimed at all those involved in the distribution of medicinal products for human use, active substances, or veterinary medicinal products. It is especially relevant for Responsible Persons (RPs), quality managers, compliance officers, and anyone responsible for ensuring GDP compliance and qualifying logistics service providers. Companies considering commercial GDP certification and seeking information on its advantages, limitations, and potential certification bodies are also addressed.
Date & Technical Requirements
Date
Monday, 03 November 2025, 14.00 – 16.00 h CET
Technical Requirements
We use Webex for our live online training courses and webinars. At www.gmp-compliance.org/training/online-training-technical-information you will find all the information you need to participate in our events and you can check if your system meets the necessary requirements to participate. If the installation of browser extensions is not possible due to your rights in the IT system, please contact your IT department. Webex is a standard nowadays and the necessary installation is fast and easy.
We use Webex for our live online training courses and webinars. At www.gmp-compliance.org/training/online-training-technical-information you will find all the information you need to participate in our events and you can check if your system meets the necessary requirements to participate. If the installation of browser extensions is not possible due to your rights in the IT system, please contact your IT department. Webex is a standard nowadays and the necessary installation is fast and easy.
Programm
Gesamtes Programm als PDF herunterladen
This webinar provides a practical and comprehensive overview of GDP certification in practice, highlighting key challenges and considerations for logistics partners and pharmaceutical companies alike.
| ECA-Member*: | € 349,- |
| Non ECA Member*: | € 399,- |
Alle Preise zzgl. MwSt. Wichtige Hinweise zur Umsatzsteuer.
* auch unkompliziert per Kreditkarte bezahlbar
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Seminarprogramm als PDF
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