Active Pharmaceutical Ingredients (API)

Aesica has over 30 years’ experience in API development, manufacturing and generic supply.

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Our capabilities in API manufacture include:

Our regulatory and support chain services include:

  • Regulatory expertise and support
  • Compilation and submission of Drug Master Files (DMF)
  • Support for IND applications
  • Technology transfer
  • Global sourcing practice
  • Raw material sourcing through local representatives
  • Import and export expertise
  • Secure storage and supply of controlled drugs

THE WHOLE SUPPLY CHAIN. SIMPLIFIED.

How Aesica can add value at every stage

Finished dose development – Finished dose manufacture – API development