Agilent SLIMS is a comprehensive laboratory management solution designed to streamline and organize lab operations. It combines the functionalities of a Laboratory Information Management System (LIMS) and an Electronic Laboratory Notebook (ELN) into a single platform. Here are some key features:

Agilent SLIMS offers flexible installation options and can either be hosted on a reliable, scalable, secure Agilent server, or with your favorite cloud service provider. It can also be installed on a server at your site. Deployment is quick and 100% remote. Once installed, SLIMS can be used with just a web browser from computers or tablets.

Save time and money with SLIMS

• Track your samples and lab resources
• Manage logistics and increase your lab productivity.
• Track any sample in your lab from reception, storage, and processing to results.
• Execute your lab operations
• SLIMS is a laboratory executions system (LES) that provides you a complete workflow solution: track every aspect of your workflow and maintain traceability from start to finish. Create protocols that easily integrate with equipment in your lab.
• Reduce human errors
• Move from a paper to a digital environment. Identify errors earlier with an interactive and intuitive interface.

Adaptable and efficient

• Integrate lab equipment
• Hardware and software do not have to be separate. SLIMS can be integrated with lab equipment to automate the user’s experience, saving time and money, and eliminating errors.
• Integrate to your existing systems
• SLIMS can interact with many business packages (such as identify management software, SAP, or billing systems) and also Agilent and non Agilent laboratory systems (such as Agilent OpenLab, iLab, the Alissa Platform, and more). SLIMS can also fully interface your existing systems with its APIs, which allow communication with third-party tools.
• Meet data integrity standards
• SLIMS provides the technical controls to securely acquire, process, report, and store data in laboratories that must follow the compliance guidelines of FDA 21 CFR Part 11, EU Annex 11, and GAMP5, as well as ISO/IEC 17025 and EPA 40 CFR Part 160.