Telemedical Innovations renewed its certificate of compliance with EN ISO 13485:2016
On November 6-7, 2023 auditors of the certification body TÜV Rheinland Poland, conducted in our company a recertification audit regarding compliance with the EN ISO 13485:2016 standard
The Telemedical Innovations delegation participated in the Health Business Innovations 2023 conference
Representatives of Telemedical Innovations Sp. z o. o. – Ireneusz Plaza (CEO) and Anna Szymura (specialist in biomedical technologies and project implementation) had the pleasure to take part in the Health Business Innovations 2023 conference
The power of innovative medicine in cooperation with the best
We are pleased to announce that as of October 1, 2021, Telemedical Innovations Sp. z o.o. became an official partner of the MedSilesia cluster.
Telemedical Innovations Sp. z o.o. and MedApp S.A. – we have signed a cooperation agreement
On September 1, 2021, Telemedical Innovations Sp. z o.o. has signed an agreement with MedApp S.A.
Our accent at MEDICA in Düsseldorf
In 2021, the global medical technology market will open its door to specialists in the tech-med industry. On November 15-18, the MEDICA fair will be held in Düsseldorf, where a variety of topics related to the latest developments in this field will be discussed. MEDICA aimed at the international arena, every year surprises with a […]
Registration of CARDIOVICE products to URPL (Office for Registration of Medicinal Products).
On May 24, 2021, the Company registered the CARDIOVICE products™ to the Office for Registration of Medicinal
Obtaining the Quality Management System certificate EN ISO 13485:2016
On May 20, 2021, the Company received the Quality Management System CERTIFICATE EN ISO 13485:2016 issued by the notified body TÜV Rheinland.
Obtaining an EC certificate confirming compliance with Directive 93/42/EEC for Medical Devices.
On May 20, 2021, the Company received the EC certificate – Full Quality Assurance System…
Completion of laboratory tests
On April 19, 2021, tests of the CARDIOVICE ECG Recorder product together with the CARDIOVICE App software for compliance with Directive 93/42/EEC for Medical Devices were completed.