Innovamed currently has the qualification of most of the facilities (IQ) of injection equipment for components of medical devices as well and has already fully completed the equipment for post-injection phases or sterile barrier packaging (welding, blistering, etc. ) and its Clean Rooms. The objective is to provide our clients with the opportunity to have the equipment and facilities ready to carry out the subsequent process validation (OQ / PQ) for any of the components produced at Innovamed.
With this, we intend to facilitate our clients compliance with the requirements based on the applicable regulations and regulations. For any queries, you can contact Aleix López, Quality Director through firstname.lastname@example.org or Eusebio Riola, Sales Director, email@example.com, who will complete all the information they require in this regard.