Currently, Innovamed has the qualification (IQ, OQ, PQ) of its manufacturing equipment for:
This being a regulatory requirement in ISO 13485:2016 and GMPs.
The objective is to provide the opportunity to our customers to have qualified equipment at Innovamed (IQ) facilities so they can perform process validation for their products (OQ-PQ phases).
For any queries, you can contact Aleix López, Quality Director, through alopez@innovamed.es or Eusebio Riola, Sales Director, eriola@innovamed.es
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