Clinical API Supply

Thanks to keen insights gained from our backgrounds in big pharma process R&D, we understand exactly what it takes to bring a compound into clinical trials.  We comply fully with all ICH and EMEA guidelines and are certified by the Swedish medical agency to manufacture GMP material for clinical trials.

Syntagon has vast experience in supplying clinical APIs and regulatory support to clients of all types, all over the world. From a few grams to dozens of kilograms. From small, low-weight molecules to large, highly complex and multifunctional compounds –  we are certain to deliver.

What we deliver: The desired quality and amount of clinical API and the supporting documentation necessary for a swift entry into clinical trials.

Read more  about our areas of expertise