Healthcare software is subject to the same strict legal requirements as traditional medical devices. Adliance undertakes the policy-based development of software that must be classified as a medical device. In addition to industry-specific programming, Adliance also contributes experience in all relevant standards and guidelines and also provides support, for example, in risk, quality management or validation.
From this work and the concrete needs of customers, the product "Akriva" was born. For pharmaceutical companies, Akriva automates the time-consuming and costly screening for (online) communication channels required by strict pharmacovigilance guidelines. This includes the timely processing of side effect reports, documentation and reporting for audits and authorities.
Services / Products:
- Guideline-compliant development of individual software as a medical device
- "Akriva" for automated monitoring of adverse reaction reports (pharmacovigilance) in online communication channels
Founder:
Gerhard Feilmayr
Dominik Flener
Hannes Sachsenhofer
