APIs & Excipients

We supply active ingredients, API intermediates, granules and pellets, and finished dosages forms (FDF) that comply with various pharmaceutical regulations (Ph.Eur., BP, USP, JP, ICH, GCC). We can also accommodate client-specific requirements.

Additionally, APIs are often being developed in parallel to the drug products and consequently their critical quality attributes (CQAs) can change with time. Unfortunately, there is often too much focus on the chemical purity of the API; forgetting that changes in particle size, shape and bulk density can be equally important to the resultant drug product. The habit of an API can also be impacted by polymorphism; for example, orthorhombic paracetamol shows improved compression behaviour compared to the monoclinic form.²