Dr Christian Grote-Westrick, B. Braun Avitum
A lot has happened since the introduction of the EU GDP guidelines. In the course of the reorganisation of veterinary medicinal product legislation, for example, measures on good distribution practice for veterinary medicinal products and active ingredients used as starting materials for veterinary medicinal products were issued by the European Commission. The U.S. Food and Drug Administration (FDA) is seeking to harmonize the requirements for wholesalers in the individual U.S. states, and other authorities have also specified their requirements and expectations for good distribution practice. In order to get an overview, this webinar was developed.
This webinar addresses itself to all, which are involved in the range of the distribution of medicinal products for human use, active substances or veterinary medicinal products.
Those are e.g. coworkers and high-level personnel from the following industries:
- Drug wholesaler,
- Logistics companies,
- Pharmaceutical manufacturers
- API manufacturers
- External warehouses,
- Further service providers offering services for the distribution of pharmaceuticals.
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