Active Pharmaceutical Ingredients (API)

Alongside our capabilities and services in the development and manufacture of APIs, we also offer a number of support services to meet the wider needs of our customers.


Our regulatory support team offer expertise in the management of all clinical trial and drug filing documentation, including compilation and submission of Drug Master Files (DMF, VMF) and support of IND applications.

A tight and controlled supply chain is undoubtedly a benefit of our end-to-end solution, and our wider supply chain management offering can also provide global sourcing practice, raw material sourcing through local representatives and import/export expertise as well as secure storage and supply of controlled drugs.


How Aesica can add value at every stage

API manufacture Finished dose development – Finished dose manufacture