Service Swiss Medtech Expo 2023

Qualification systems and equipment

EXCO specialists advise on all questions concerning the qualification of equipment, systems and plants for the manufacture of medical or pharmaceutical products. Ensure conformity according to the valid GMP, ISO or FDA regulations!

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.

Related topics (3)

Further applications

204 items

Regulation

94 items

Consulting

75 items