15 May 2018, 10:00-17:00


Fecc offices, Rue du Luxembourg 16b, B-1000 Brussels

Target audience

Professionals working in the supply chain of pharmaceutical starting materials.


The current medicinal products regulatory framework in Europe sets additional legal requirements to ensure the quality and traceability of pharmaceutical starting materials. GMP and GDP, as well as supplier audits and appropriate oversight on the supply chain, have become more challenging than in the past. In order to achieve this compliance, suppliers, distributors and pharmaceutical companies share responsibilities that need to be properly managed through the entire supply chain.

With this workshop distributors, as the link in the supply chain, will be informed about existing tools helping to manage challenges under the starting materials legislation.


Workshop brochure

Workshop Report

Workshop report