Patient friendly
therapies for
quality of life
Medinice S.A.
Medinice S.A. is a Polish company founded in 2012 operating in the medical technology industry. The company was established to develop new ideas for medical devices, thus meeting the needs of the market. The company is involved in the creation, development and commercialization of minimally invasive solutions in the field of cardiology and cardiac surgery that improve the quality of life. Medinice’s portfolio currently includes several projects at various stages of development. All medical devices developed by Medinice will improve the quality of life of patients around the world.
Value Creation
The value of Medinice’s developed projects is growing exponentially. After successfully completing each stage (milestone), the probability of commercialization in the MedTech industry increases significantly, which increases the valuation.
Development
In Medinica S.A. we are aware of the uniqueness of each solution. The development of the devices is based on the knowledge of the Scientific Council, which includes world authorities in the field of cardiology and cardiac surgery, and on the potential of the Medinice team consisting of experienced engineers and experts. The team’s extensive qualifications allow us to minimize the risks associated with the R&D process.
Research
Based on our current experience and the adopted development direction, we cooperate closely with leading scientific units, research institutions, hospitals and certified laboratories where our medical devices are tested.
Commercialisation
The key source of the Company’s revenues is the commercialization of developed solutions. Our team has experience in capital exits and intellectual property sales. The company establishes relationships with leading global manufacturers of medical products.
Certificates
Medinice S.A. has an ISO 13485 certificate issued by a notified body in the field of design, development and production of active medical devices. Compliance with this standard means that the Company has implemented a quality management system for medical devices, i.e. the Company has documented processes and procedures allowing it to achieve quality assurance goals. Meeting these requirements allows you to apply for marketing authorization for medical devices.
