Qualification systems and equipment

Maintain compliance according to applicable GMP, ISO or FDA regulations and requirements:

• Qualification in the clinical environment
• Equipment qualification for medical devices, active ingredients and pharmaceutical products
• Equipment qualification (equipment, workbenches, incubators, isolators, particle counters, refrigerators and freezers, cryostorage, etc.)
• Cleanroom qualification
  
  

Visit us at SMTE 2023 on September 12 and 13 or already now on our website: www.exco-consulting.ch.