• Drug substances and products: small molecules and biopharmaceuticals in various dosage forms (solids, semi-solids, liquids and injectables)
• Excipients analysis as per USP, Ph.Eur. and JP
• Intermediates & Starting materials
• Packing material testing as per USP and Ph.Eur.

According to either compendial methods (USP, Ph.Eur. and JP), Sortis pharma proprietary method or your method. We can transfer validated analytical methods to or from your site, according to the formal process of the ICH guidelines. Alternatively, the methods can be developed and validated at Sortis pharma or are routine methods already in place at Sortis pharma or requiring verification only.