Medical Laboratory Software

Intellitec develops powerful and reliable laboratory middleware solutions providing connectivity, workflow support and data management allowing laboratories and doctors to improve their processes and to diagnose and treat patients more effectively

We are Experts in:

Middleware, Core Lab, Clinical Chemistry, Microbiology, Point of Care Testing, Hematology, Connectivity, Data Management, Rule Engine, Auto Verification, Reflex Testing, Order Entry, Quality Control, Workflow Support, Reporting, ASTM / CLSI LIS, HL7, ISO 9001, ISO 13485, IEC 62304, ISO 14971

Our customers are leading international manufacturers in healthcare diagnostics and clinical information system vendors.

Hospitals, medical laboratories and resident physicians in more than 500 installations and across more than 30 countries successfully use middleware systems developed by Intellitec for their daily routine.

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Intelligent middleware solutions from Intellitec can provide a versatile response to a variety of challenges in the medical laboratory

aurelio/lab is a powerful and flexible laboratory middleware solution providing extensive connectivity, data management and workflow support features for making lab processes more efficient, reducing errors and improving quality so users can concentrate on important tasks that need their attention.

Based on aurelio/lab Intellitec has developed solutions for clinical chemistry, microbiology/bacteriology, hematology, specialty testing and point-of-care (POC) test management.

Furthermore, Intellitec has partnered with a number of instrument vendors to provide special editions and branded customer solutions.

Regulatory and Quality Management

Intellitec has long-term experience with managing software projects in compliance with national and international quality system regulations and standards, such as EU IVDR, MEDDEV, ISO 13485, ISO 14971 and IEC 62304.

We have developed a quality management system that fully integrates the requirements of ISO 9001:2015 and even meets the advanced requirements of ISO 13485:2016 for medical device manufacturers. Periodic and independent audits through a ISO accredited certification body have confirmed that these procedures are appropriate and effective the work we do for our customers.

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Feel free to get in touch if you have any questions or suggestions


Wilhelmshöher Allee 306B
34131 Kassel