Development Services

Aesica offers API and finished dose development as part of our full service, end-to-end pharmaceutical development and manufacturing solution.

In API development, we offer complementary services in research and development and clinical supply, supported by experience in regulation and documentation.

In finished dose, we have capabilities and expertise in formulation development, clinical batch manufacturing, and clinical trial supply.

Through our dedicated project teams, we focus on building strong customer relationships founded on good communications and approachability, while our knowledge, experience and world-class facilities ensure all projects are delivered fully, on time, and to budget.

All our  pharma development services services are supported by our proven track record for quality and regulation, including MHRA and FDA approval, and our rigorous health and safety processes.

Click here to find out more information about our Finished Dose or API development capabilities.

THE WHOLE SUPPLY CHAIN. SIMPLIFIED.

How Aesica can add value at every stage

API development API manufacture Finished dose development – Finished dose manufacture