Safe routines regarding medical devices create security for patients, users and staff. With the right support, MDR becomes an opportunity to improve quality – not a burden.
As a unit manager, you bear the ultimate responsibility for compliance
Requires medical devices to be safe, effective and traceable throughout their life cycle.
Specifies healthcare providers' obligations: procedures, training, documentation, traceability and reporting of deviations.
Lack of compliance risks patient safety and the confidence of supervisory authorities.
Obstacles that make effective management of medical devices difficult
Excel sheets and binders are difficult to keep updated and accessible to the entire organization.
Staff lack access to instructions for use and important product information when they need it.
Difficult to get a comprehensive picture of the operation's medical devices - which leads to unnecessary costs.
Deviations and incidents are reported late or not at all due to cumbersome processes.
From regulatory compliance to improved quality and more time for patient care
Full control over products, costs, expiration dates and service history via QR codes and Alisa's digital system.
Centralized instructions and documentation in app format for all staff.
On-site documentation of inspections and incidents frees up time from administration.
Automatic compliance with MDR and Swedish regulations, reduced risks and more time for patient care.
Contact Alisa to simplify regulatory compliance and focus on what really matters
Contact us