ISO 17025 -standard
The ISO 17025 standard describes the general and technical requirements for the activities of testing and calibration laboratories.
The ISO 17025 standard describes the general and technical requirements for the activities of testing and calibration laboratories. Compliance with the standard indicates that the organisation is capable of competent, impartial and consistent operation.
Kasve’s specialists are experienced in designing, constructing, updating and auditing ISO 17025 compliant quality management systems. We will help you with your quality management needs at the different project stages. Our experts have obtained qualifications to perform technical assessments in a training provided by FINAS.
Looking for a quality expert?
We have helped a number of medicinal device manufacturers, testing and clinical laboratories, and start-ups develop their operations.
IEC 60601 -standard
IEC 60601 is a series of technical standards that describes the requirements for the safety and essential performance of medical electrical equipment.
IEC 62304 -standard
IEC 62304 defines the set of processes for life-cycle management of medical device software.
ISO 13485 -standard
The ISO 13485 standard sets a frame for quality management systems for both medical device manufacturers and other organisations in the chain.