The FHIR standard for healthcare interoperability is gaining popularity due to its numerous benefits. With the aid of the FHIR standard, social and healthcare information systems can be implemented gradually. Next, we describe some of the benefits of the FHIR…
Healthcare resources are severely stretched. And although a lot of patient data has been collected, making use of it is difficult. New tools are needed to ease the workload of healthcare personnel. This is where artificial intelligence comes in: AI…
Diagnosing concussions is complicated, as it is often based on the patient's subjective experience. Atostek has been involved in developing a platform that enables reliable concussion diagnosis. In addition, Atostek's medical device know-how played an important role throughout the development…
With the nationwide reforms of Finland’s health and social services sector, the wellbeing services county system will become operational in 2023. The reforms also include significant changes in information and communication technology. What can agile software companies offer, and how…
Atostek has signed a global partnership agreement with an American company Tala Secure. Together, the two companies offer a 1-stop-shop software resource for medical device companies and institutions with integrated and connected healthcare needs. The purpose of the cooperation is…
Seamless cooperation between the authorities and the business world ensured that the nationwide Covid certificate service was completed within a month. Provided for nation-wide use by THL and implemented by Atostek, the EU Covid vaccine printing and recording service was…
Atostek has started a joint research project with Shanghai Jiao Tong University. The aim of the research project is to develop algorithms that predict cancer. The joint research project between Atostek and the Chinese university aims to promote international collaboration…
Preparations for anesthesia typically entail filling in paper forms and checking patient data in multiple systems. However, thanks to innovative software created in cooperation Atostek and Pirha, that is becoming a thing of the past. The AneDigi program combines data…
The development of a medical device or software is regulated in Europe by the Medical Device Regulation (EU 2017/745). Then again, MDR does not really involve much extra work to software development – compared to what it should be anyway.…
What are the most important things to consider in planning and implementing effective and standard-compliant testing of medical software? By medical device we mean, for example, a device or software that is used to diagnose or treat patients. The software…
