Usability and security result in a new LIMS standard: MAQSIMA LAB+.
MAQSIMA LAB + was developed from customer requirements and is optimally adapted to the individual processes in the laboratory, which is particularly reflected in the acceptance and satisfaction of the users. LIMS provides all the functionality that a LIMS needs to process samples in compliance with national and international guidelines. Goods receipts and production orders automatically trigger the generation of samples to the desired extent. MAQSIMA LAB + report releases or block connected systems (e.g. ERP systems). In addition to the central LIMS functions, MAQSIMA LAB + has a large number of specific modules that are ideal for the implementation of the most diverse, often industry-specific laboratory processes. The modular system structure enables the specific alignment and scaling of the system to the company's requirements. If necessary, for example, tests such as drug release, uniformity of content or mass, impurities or complex tests (e.g. drying loss) from the policy can be efficiently implemented with the process control inspections in the system. MAQSIMA LAB + offers policy compliance with GxP and FDA Regulation 21 CFR Part 11. With its extensive role-based user and rights management, as well as access protection and audit trail functionality, LIMS also ensures safety and transparency in the laboratory.