Autoscribe Informatics
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Autoscribe Informatics software

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Regulated Laboratory LIMS Solution

Fast Deployment LIMS Solution; Fast deployment is a key benefit of Matrix Express LIMS. Easy configuration means that you will quickly start to benefit from this LIMS solution as it requires minimal resources to implement. The system includes user defined fields and a series of ready-to-use reports that are suitable for most application areas. It will help you meet the requirements of a regulated laboratory, working to standards such as FDA 21 CFR Part 11, UKAS and GLP.

Matrix Hazardous Waste Tracker LIMS

Matrix Hazardous Waste Tracker is designed to track, locate and consign any type of hazardous waste samples anywhere in an organisation for compliance with regulatory authority legislation. Applications include the tracking of nuclear waste, biohazard waste from hospitals and veterinary practices and waste electrical equipment (WEE).

Forensic Systems LIMS

Matrix Gemini and Matrix Tracker software are highly configurable and can be used to meet the specific requirements of a forensic system both in terms of managing the laboratory information and storage and tracking of evidence.

Autoscribe Xybion LIMS - Laboratory Information Management System

Improve efficiency, automation and turn-around times in busy laboratories by tracking samples, managing data, whilst reducing errors with a fully featured LIMS. Track samples, manage data and reduce errors in busy laboratories. Use how you like: Xybion LIMS uses a web browser interface. It may be deployed on a local server or be cloud based, for maximum flexibility. Use across the organization: The point and click configuration makes Xybion LIMS quick to configure, easy to learn and easy to update with no coding skills needed. Use without limits: Accommodate change, meaning a long system lifetime and lower cost of ownership. It`s also scaleable - from a single user to global usage, with fast and cost effective implementation. Achieve compliance: Configurable workflows and third party access provision means processes are upheld, authorities gain access to verify tests and standards including ISO17025, GMP, GLP and FDA 21CFR Part 11 are met.