Matrix Gemini LIMS for the Pharmaceutical Industry
Matrix Gemini is a fully configurable solution for pharmaceutical companies. Matrix Gemini is suitable for all types of laboratory from QA/QC laboratories, stability testing and R&D laboratories to laboratories analysing clinical trials of novel pharmaceuticals. Particularly important to the pharmaceutical industry is compliance to guidelines including the FDA's 21CFR Part 11 that require change control, validation and audit trailing of changes to the system and the data that it holds.
Using the unique built-in configuration tools Matrix Gemini can provide a match to the specific requirements of each laboratory in terms of workflows, tests, terminology and reports. We have a specific stability management module to track samples undergoing stability trials. It manages the study protocols, the pull points, the inventory of samples, storage chambers and the tests required for each sample.
Matrix Gemini has a dual user interface, it can be accessed through the desktop client or a browser - you can choose the connection to suit your situation and role. If you are out of your lab today, use the Web; back in tomorrow use a client on your LAN. Today, laboratories must be able to change their processes and workflows and their LIMS must stay in step with these changes. This is a challenge for a LIMS solution, unless the system is extremely configurable. Matrix Gemini offers fast implementation and an excellent fit to specific user requirements, by utilising our configuration tools, for a wide range of laboratories and processes.
Matrix Gemini lets you easily manage:
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For information on Pharmaceutical Stability Protocol Management
