GMP, GDP, and GCP are directly interconnected when it comes to clinical trial medicinal products. Especially in packaging, labeling, storage, as well as import and export, regulatory requirements must be reliably translated into practical procedures.

This is precisely where our hybrid seminar "Clinical Trials with Investigational Medicinal Products: GMP and GDP" comes in: on November 11-12, 2026, in Alzenau or online.

In addition to the regulatory fundamentals and practical workshops, participants attending on-site will experience a special highlight: a visit to the packaging and storage center of Prestige Promotion in Alzenau. You will gain insights into the practical implementation of packaging, labeling, and temperature-controlled storage of clinical trial medicinal products.
The topics of focus include among others:

- GMP and GDP requirements for investigational medicinal products
- Packaging and labeling according to CTR
- Import and export, including customs aspects
- Logistics and storage of clinical trial medicinal products
- Concrete case studies and workshops

Secure your spot here and experience GMP and GDP in clinical trials firsthand: Clinical Trials with Investigational Medicinal Products: GMP and GDP on November 11-12, 2026

If the perspective of clinical study data is also relevant for you, I recommend our webinar package: Navigating Clinical Research with Data Science. It covers the setup and process of clinical trials, data management and analysis, up to the regulatory-compliant use of modern data science and AI methods.