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A UL course

This course describes the Good Distribution Practices required by the European Union (EU). The EU’s recommended practices are similar to requirements in the U.S. and many other countries. The controls to maintain the quality and integrity of medicinal products as they are distributed from manufacturer to patient are explained in this course. Because modern supply chains are often complex, the responsibilities of all organisations involved with wholesale activities — including storage, transport, purchase, and supply — are detailed. The controls required to prevent falsified or fake products entering the supply chain are also addressed.

Featured topics

  • Botanical drug products (BDPs)
  • Cell culture
  • Antibody production
  • Early intervention programs
  • Processing and packaging
  • Controls and testing

Who should attend?

Professionals and experts in the pharmaceutical, biotechnology, and medical device fields

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