slp.blue®
Documentation and quality management system you can rely on at audit time.
slp.blue® is a modern web application for documentation and quality management. It automates the administration associated with quality management standards (ISO 15189, 17025, 13485, 9001, and IVDR/MDR), saves time, and keeps your documentation interlinked, up to date, and always audit-ready.
slp.blue includes complete functionality for electronic document management, including version control for individual documents, management of the review and approval process for new versions, setting validity dates, and managing the process of familiarizing users with document changes. It also supports printing documents, including formal elements such as a cover page and header, as well as subsequent management of individual printed copies (e.g., copy number, quantity, location, version, and owner).
Why choose slp.blue
Seamless Compliance with ISO 15189:2022 and IVDR
- Fully aligned with ISO 15189:2022
- Whether you are new to ISO or upgrading from ISO 15189:2012 — we make the transition simple
- Ready to support your IVDR implementation
- Printing optional — fully compliant without paper
Smart Electronic Document Management
- no formatting issues nor compatibility problems
- documents stay interconnected, structured and always up to date
- user acknowledgment of document changes built-in
- full-text search across documents — not just titles or tags.
Method Management, Verification & Quality Control
Supports integration with local, national, and international laboratory coding standards — automatically updated and fully structured.
Comprehensive Quality Management Modules
- Personnel and training records
- Laboratory equipment and software
- Suppliers and their related agreements
- Risk assessments
- Nonconformities, potential improvements
- Audit planning and recording
Create Your Laboratory Web Presentation Instantly
Fast and Painless Onboarding
Whether you manage your documents using Word or another system, we migrate everything, including metadata. AI helps us to extract the data from any document format and system. We’ll even help you clean up and organize your existing documentation during the migration. Automated processes in slp.blue then keep your documentation clean and consistent — forever.
Access from Anywhere
Friendly Licensing and Ongoing Support
- Unlimited users, unlimited documents — no hidden fees or restrictions
- Automatic updates every 3 weeks with minimal downtime
- Live webinars and user feedback driving slp.blue forward
- Responsive support — we resolve issues fast because we know speed matters
Cloud or On-Premise? You Choose.
- Connect to your Laboratory Information System (LIS), Electronic Healthcare Record system (EHR), or any other software in your infrastructure — our open API makes it possible.
- Enable single sign-on (SSO) with your existing user management system
References
RNDr. Tomáš Gucký, Ph.D.
Vladislava Jamriková
Ing. Aleš Troszok, Ph.D.
Ing. Alena Kameníková
RNDr. Iveta Nedvědová, Ph.D.
Ing. Václav Senft
Our Customers
slp.blue is deployed across a wide range of specialties:
- 54× clinical biochemistry
- 39× hematology
- 20× medical microbiology
- 21× transfusion medicine
- 16× allergology and immunology
- 12× pathology
- 7× medical genetics
For Transfusion Centers and Blood Banks
slp.blue® also covers the specific requirements of transfusion workplaces — documentation and quality management in accordance with Good Manufacturing Practice (GMP) and readiness for regulatory oversight under the regulation on human blood. Today, more than 20 transfusion workplaces use the system.
Laboratory Handbooks
Our customers like to use the dynamic laboratory manual feature because it allows them to always have up-to-date information in one place, easily share it via a unique URL, and do so without any involvement from the IT department.
IKEM
Centrální laboratoře FNKV
Ústav patologie FNKV
OKL Masarykovy nemocnice Rakovník
Laboratoř Krevního centra
OKBH Nemocnice Vrchlabí
OKB Nemocnice Pelhřimov
OKBMI Nemocnice Jihlava
OKB Levitova centra následné péče
Team
Tomáš Kouřim
CEO and co-founder of Mild Blue
slp.blue development coordinator
Jan Kubant
CTO and co-founder of Mild Blue
Project manager of slp.blue
Ing. Jakub Monhart
slp.blue Developer
Business Development Manager
Jan Skála
Responsible for DevOps, backend development, and slp.blue architecture
Iva Zajacová
COO
Invoices, contracts, training organisation, data import and administrative support for migrations
Lubomír Šotek
Senior Business Developer
Pavel Mach
Head of Deployment, Instructor and Developer
Zuzana Červínová
Support, Developer and Content specialist
in cooperation with
Antonín Jabor, Ph.D.
Deputy Head and Head of the Central Laboratory, Department of Laboratory Methods, IKEM Hospital, Prague
Head of the National Center for the Authorization of Clinical Laboratories
Jiří Kotrbatý
Quality manager and Head of the Central Reception of Samples, Department of Laboratory Methods, IKEM Hospital, Prague
Co-author of the SLP® system
Miroslav Zámečník
Co-author of the original SLP® system
Administrator of the National Laboratory Items List and Czech Medical Data Standard
Luděk Straka, Ph.D.
RNDr. Luděk Straka passed away on June 17, 2023, at the age of 60. We remember him as the main creator of the original SLP® system.
Want to learn more?
Contact us
Would you like to explore how slp.blue could be utilized in your laboratory? Feel free to contact us via e-mail at [email protected] or simply fill out the contact form below and we will get in touch with you soon!