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Compliance made easy in the lab

Strict pharmaceutical regulations require seamless documentation and GXP/FDA as well as ISO 17025 compliance. iLIMS offers a comprehensive system for efficient processes and combines laboratory management with CRM, sales, project management, and accounting into an integrated solution for maximum efficiency and transparency.


Features

Key Features for Medicine and Pharma

Central key features of iLIMS Pharma are pharmacopoeias for testing methods, customizable limits, audit trails with justification, multi-level approvals, as well as SOP, skill, and batch tracking. Complemented by CRM, project management, and accounting, these optimize seamless processes in pharmaceutical laboratories – GxP certified since 2019 by PTA.

Microbiology

  • Recording and documentation of microbiological approaches with material-dependent dilution levels

  • Determination of the nutrient medium requirement per approach

Pharma

Report Designer

  • Creation of test reports, accompanying documents, delivery notes, and certificates

  • Integration of digital signatures for legal certainty

Extensions

  • Photodocumentation from sample receipt to result transmission

  • Extensive evaluation options with statistics, pivot tables, and graphics

LaborgerÀteanbindung

Laboratory Equipment Connection

  • Device server (iCONTROL) for digital, networked, and automated laboratory

  • Increase in efficiency and quality of laboratory work through automation

GerÀte im Labor
GlÀser im Labor
Why device connectivity in the laboratory is essential

Our device server iCONTROL

A central aspect of laboratory digitization is the seamless integration of your laboratory devices into the lab management ecosystem. With our iCONTROL, we provide you exactly that – a powerful tool that connects your laboratory devices effortlessly to your LIMS.

Dialog

How iLIMS supports laboratory operations

iLIMS is the flexible laboratory information and management system that supports your team in all processes. Thanks to its modular structure, you decide which components to use – perfectly tailored to the needs of your laboratory. This creates efficient workflows, increases quality, and keeps you in full control of your data at all times.

Labor Manager

What exactly does your industry solution for pharmaceutical laboratories offer to ensure compliance?

Your Consultant INTEGRIS LIMS

Our iLIMS solution is qualified according to GxP and FDA and ensures the highest security with password prompts for sensitive functions and an extended audit trail. Changes are documented with justifications.

Labor Manager

That sounds good. How do you support the management of complex compositions?

Your Consultant INTEGRIS LIMS

We represent complex mixtures such as preparations, formulations, or raw material mixtures in detail. Additionally, we offer safety features such as RFID login at the workplace and automatic logout.

Labor Manager

How is user access regulated?

Your Consultant INTEGRIS LIMS

Permissions are based on qualifications and proof of knowledge of SOPs. Furthermore, you maintain standards, regulations, and instructions centrally and manage user rights very flexibly through roles and permissions.

Labor Manager

What additional modules do you recommend for pharmaceutical laboratories?

Your Consultant INTEGRIS LIMS

For microbiology, we offer the recording and documentation of microbiological approaches with variable dilution levels and automatically determine the nutrient medium requirements. Our laboratory device connection via the iCONTROL device server enables a connected, automated laboratory.

Labor Manager

And what about documentation and evaluation?

Your Consultant INTEGRIS LIMS

With the report designer, you create test reports, accompanying documents, delivery notes, and certificates – of course, also with a digital signature. Additionally, you can document photos from sample receipt to result and perform extensive evaluations via statistics and pivot tables.

Labor Manager

That sounds like a very comprehensive solution.

Your Consultant INTEGRIS LIMS

Exactly, iLIMS offers everything laboratories in the pharmaceutical sector need to comply with compliance, security, and efficiency.

Secure and verifiable: iLIMS meets ISO 17025 and is ISO certified

iLIMS supports laboratories in implementing regulatory requirements – from audit trails to electronic signatures. Optionally, we provide prepared validation documents according to GAMP 5.

ISO 17025
Autonomer Löslichkeitstester im Pharmalabor
Versuch im Labor

Ready to improve your lab processes?

Schedule a demo for our lab software today! We look forward to showing you the features and benefits.