We help healthcare organizations grow their own expertise and develop and commercialize products with both individual and societal significance.
Take over the digital revolution in healtcare industry
Kasve is committed to embracing new technologies and modern methods to operate more efficiently. This will ensure that your product is brought to market as quickly and cost-effectively as possible.
From idea to market
We offer a unique combination of in-depth understanding of regulations and quality management in our industry, combined with solid expertise in business development.
Quality Assurance and Regulatory Affairs
Software Life Cycle Management
TopExpert Recruitment Trainings
Trainings for Quality Professionals
Do you need a qualified partner to support you?
We help healthtech companies succeed in the international market. Leverage our expertise and our comprehensive network!
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.
ISO 14971 -standard
ISO 14971 is a key risk management standard for medical device manufacturers.
ISO 15189 -standard
ISO 15189 is the quality management standard for medical / clinical laboratories, which places the patient care perspective at its centre.
ISO 17025 -standard
The ISO 17025 standard for testing and calibration laboratories describes the general and technical requirements for the competent, impartial and consistent operation of laboratories.
ISO 27001 -standard
ISO 27001 is an internationally well-known information security standard.