ATMP regulatory guide
This regulatory guide will provide useful information and insights throughout the Advanced Therapy Medicinal Product development process and help you through the important steps from process development to clinical use. In this guide you have the possibility to navigate through the general steps for clinical trial and all the different classifications.
Contact Läkemedelsverket or the European Medicines Agency (EMA) at an early stage for advice on your process development plan.
For more information on the guide or for comments and suggestions please contact Ann Novotny
You can learn more about the Swelife-ATMP regulatory project that are developing these resources under Swelife-ATMP Projects