Pharmaceutical LIMS software: protect your data integrity
Dedicated to the pharmaceutical sector, AQ Manager LIMS oversees your analyses and secures your data, thanks to configurable workflows that adapt to your working methods.
The advantages of LIMS for the pharmaceutical sector
AQ Manager LIMS strengthens data and process control within pharmaceutical laboratories.
Meet your regulatory requirements
Meet the requirements of GMP, ISO 9001 or 21 CFR Part 11 more easily thanks to rigorous data management.
Preserve the integrity and traceability of your data (Audit Trail)
Centralize your data in a secure environment where every entry, modification, deletion, and validation is automatically recorded. The integrated Audit Trail guarantees even more complete traceability.
Enforce your standardized procedures
Automate the application of your standard operating procedures (SOPs) to guarantee consistent execution of analyses and limit errors.
Reduce manual tasks and the risk of error
Automatically import data from your instruments and reduce manual re-entry to improve the reliability of results and decrease the time spent on verifications.
Tailor-made features for your teams
Sample and batch management
Identify each sample and each batch, track their life cycle and progress, from reception to the end of analysis, with complete traceability.
Document management
Link each document (SOP, methods, certificates, protocols, etc.) to any type of record, with version control and revision alerts to ensure you are always working on the correct version.
Results entry and non-conformities
Enter your analysis results and automatically manage out-of-specification results (incident notes) to make each of your decisions more reliable and secure.
Retesting and stability studies
Track the evolution of your products thanks to retesting plans defined in your analysis profiles. Automatically resubmit your samples for analysis at the scheduled intervals and receive an alert to verify continued compliance.
Discover all the features of our LIMS to optimize your laboratory management
A LIMS software for all laboratories in the pharmaceutical sector
Quality control laboratories
Control your raw materials, products in progress, and finished products to guarantee their compliance.
Bioanalysis laboratories
Perform and track your biological analyses with complete traceability and in compliance with regulatory requirements.
R&D laboratories
Support the development of your new products and the monitoring of their quality.
Manufacturing process control laboratories
Monitor analyses during production and control quality at every stage of the process.
Service provider laboratories
Manage your entire activity, from your clients’ analysis requests to the delivery of results.
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AQ Manager LIMS, the benchmark for the pharmaceutical industry
Here are four additional reasons to trust us.
A simple interface with adjustable graphic menus according to each user profile facilitates navigation, reduces learning time, and encourages adoption of the tool.
Our client case studies in the sector
AQ Manager LIMS vs. a standard LIMS
Would you like to learn more about the LIMS dedicated to pharmaceuticals? Consult our brochure
Frequently asked questions
A LIMS (Laboratory Information Management System) is a software solution that centralizes and automates all operations within your pharmaceutical laboratory. It offers an alternative to paper documents and Excel spreadsheets, which are often prone to errors, while guaranteeing data reliability, securing quality controls, and helping the laboratory comply with normative and regulatory requirements.