CEFALY Technology innovates in the medical domain with as main objective the Therapeutic Progress. This means that the new products must bring a benefit to the patients in comparison with existing treatments. The activity is therefore driven by patient’s interest and not by the search for market shares by developing «me-too» drugs or devices.
The Therapeutic Progress can address the efficacy of the treatment in clincal practice, on the reduction of side effects, on the convenience of use or on the reduction of cost to the society and to the patients.
Quality and safety are key aspects of CEFALY Technology’s core values. A comprehensive quality management system has been introduced and is constantly updated.
All products of CEFALY Technology bear the CE mark for the medical devices.
CEFALY Technology is ISO certified : Design, development and production processes comply with the strictest quality standards:
- ISO Medial 13485 : 2012 (QUALITY SYSTEM SPECIFIC TO MEDICAL MATERIALS)
- ISO13485 under CMD CAS
- ISO 9001 : 2008 (COMPREHENSIVE QUALITY SYSTEM)
- GMP (GOOD MANUFACTURING PRACTICES)
- GCP (GOOD CLINICAL PRACTICE)