Scantox has GMP manufacturing facilities for oral and topical products as well as suppositories and inhalation solutions, and perform GMP manufacture for Clinical Phase I and Phase II in our GMP approved suites.

We are certified by the Danish Health Authorities for GMP manufacturing, primary and secondary packaging, Quality Control testing and QP certification of Investigational Medicinal Products (IMP) and Quality Control testing of marketed products.

Our service portfolio includes:

• GMP manufacturing of oral and topical products
• QC release testing and QP certification of Investigational Medicinal Products >> Learn More
• Primary and secondary packaging
• Distribution of Investigational Medical Products to clinical sites at controlled conditions
• Scale-up of manufacturing process
• Technology Transfer of manufacturing process to CMO for commercial manufacture
• Stability testing in accordance with all ICH conditions and regulatory guidelines to establish shelf life of product >> Learn More
• Return of IMP, reconciliation and destruction