EU Commission publishes Feedback on New Good Distribution Practices (GDP) Guide

Recommendation
9 September 2025
Basel, Switzerland
Specifics in the Distribution of Medicinal Products
Directive 2011/62/EU against counterfeit medicines plans the creation of guidelines for good distribution practice. The existing guideline from 1994 on good distribution practice (Document 94/C 63/03) cannot be used as it has become outdated with regard to the general progress made in good storage and distribution practice. Therefore, an in-depth revision had to be performed. On 15 July 2011, the EU Commission published the revised draft on good distribution practice with a deadline for comments until 31 December 2011 on its website (see also our News from 20 July 2011).
On 1 February 2012 the Commission published the comments received from authorities, associations and industry - including transport and logistics companies - without any thematic structure. In total, there are 82 single PDF documents which can be read on the Commission Website in the section "Public Health".
Author:
Dr Gerhard Becker
CONCEPT Heidelberg (a service provider entrusted by the ECA Foundation)
Related GMP News
10.06.2025Stimuli Article Proposes Revision of USP Definition of Controlled Room Temperature (CRT)
10.06.2025New MHRA Blog Post: Supplying Medicines to Ships, Aircraft and Oil Platforms
10.06.2025Questions and Answers from the ECA Webinar "GDP Update 2025" - Part 3
10.06.2025Meet the GDPA Board Members at the GDP Forum in Barcelona
10.06.2025Swissmedic Technical Interpretation: What Counts as a Major Change in GDP?
10.06.2025MHRA informes about Validity Date of UK issued GDP Certificates