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 sector. The company was established to develop new ideas for medical devices to meet market needs. The company is engaged in the creation, development and commercialisation of life-enhancing, minimally invasive solutions in the field of cardiology and cardiac surgery. Medinice’s portfolio currently includes more than a dozen projects at various stages of development. All of the medical devices developed by Medinice improve patients’ lives and are widely used around the world.
Value growth
The value of the Medinice projects under development is growing exponentially. Upon successful completion of each stage (milestone), the probability of commercialisation in the MedTech industry increases significantly, which drives up the valuation.
Development
At Medinice 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 the potential of the Medinice team of experienced engineers and experts. The broad qualifications of the team allow us to minimise the risks associated with the R&D process.
Research
Based on our experience to date, as well as our adopted direction of development, we maintain close cooperation with leading scientific entities, research institutions, hospitals and certified laboratories where our medical devices are tested.
Sales
A key source of revenue for the Company is the commercialisation of developed solutions. Our team is experienced in equity exits and the sale of intellectual property. The Company establishes relationships with leading global medical product manufacturers.
Certifications
Medinice S.A. is ISO 13485 certified by a notified body for the design, development and manufacture 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 to achieve its quality assurance objectives. Meeting these requirements makes it possible to apply for marketing authorisation for medical devices.
