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Industrial Area

API introduction in a multiproduct facility

With the business opportunities arising from the possibility of including a new product in a pharmaceutical plant, quick and clear responses are required on whether the product may or may not be manufactured.

At Azierta, we develop a customised process for each client to define whether the product can be manufactured or whether its manufacture requires the previous implementation of any technical of administrative measures.

We work in conjunction with prestigious laboratories to develop an objective and scientific system:

api introduction in a multiproduct facility

What do we check on the process  of Incorporation of API?

  • We ensure regulatory compliance in line with the most up-to-date current regulations.
  • We maximise personnel protection in the plant in line with the API risk.
  • We have toxicologists specialised in toxicological evaluation to guarantee the viability of the manufacture of each API.

Multidisciplinary team of expert toxicologists accredited by AETOX, EUROTOX and ERT.

Leading innovation in pharma & health

100 professionals

Over 100 professionals

500 clients

Over 500 clients

9 year experience

9 years of experience


Leading innovation

Client oriented

100% client oriented


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