This webinar is designed for all professionals involved in the distribution of medicinal products for human use, active substances, and veterinary medicinal products. It is particularly relevant for employees and senior personnel from the following sectors:
Drug wholesaler
Logistics companies
Pharmaceutical manufacturers
API manufacturers
External warehouses
Further service providers offering services for the distribution of pharmaceuticals
Objectives
Good Distribution Practice (GDP) comprises measures within the pharmaceutical supply chain to ensure the quality and integrity of medicinal products and active pharmaceutical ingredients (APIs). Regulatory requirements for the distribution of medicinal products and APIs have steadily increased, affecting not only storage, transport, and distribution companies and wholesalers but also manufacturers. To meet these growing demands, regular training for all stakeholders is essential.
In recent months, there have been numerous updates and innovations in the field of GDP. This webinar has been designed to provide a structured and comprehensive overview. It includes a presentation followed by a Q&A session, allowing participants to address their questions.
Programme
This webinar aims to give a comprehensive yet compact overview of current requirements and latest developments in GDP – those already realized and those planned:
Regulatory updates – Changes in regulations, guidelines, and publications from authorities and organizations over the past 12 months
Insights from the European GDP Association
GDP Compliance – Overview of key requirements, responsibilities, and essential documents/SOPs
GDP Non-Compliance Reports 2025 – Key findings and preventive measures
Lessons from GDP inspections – Common pitfalls and how to avoid them
Outlook for 2026
Further Information
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.
The Q&A session is included and will also be provided in written form.
Fees (plus VAT) Single participation: € 349.- for ECA Members € 399.- for non-ECA Members
(This fee does not include the ECA Membership. You will find more about the ECA Membership at www.gmp-compliance.org/about-the-academy.) Group Participation (fee per person): 3-10 Persons € 359,10 11-20 Persons € 319,20 more than 20 Persons € 279,30
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.
Conference language The official conference language is English.
Testimonials
