Autoscribe Informatics will again be exhibiting at the Making Pharmaceuticals event, giving visitors from the pharmaceutical industry the chance to see how the Matrix Gemini LIMS can help streamline business, increase profitability and meet regulatory requirements. On show will be Matrix solutions in the key areas of stability studies and environmental monitoring, as well as the powerful and versatile Matrix Gemini LIMS.
Held over two days, Making Pharmaceuticals is one of the largest pharmaceutical conferences in the UK. Free to attend conference sessions are supported by more than 200 exhibitors to cover topics from research to the production of pharmaceuticals and medical devices.
Matrix Gemini Stability helps to simplify the whole stability study management process, which can be complex and time consuming for multiple studies. The fully configurable, built-in stability study management functionality is designed to automate and control the entire operation of the stability study including: protocol creation, study initiation and management, inventory management, sample pull points, future workload reporting and stability study reporting.
The Matrix Gemini Environmental Monitoring solution provides a robust framework for regular testing for contaminants at strategic locations such as air vents, bench tops and filling machines in production areas. The tests (and associated limits) and testing frequencies required for each sampling paoint can be defined. The system then uniquely links sampling point locations, test results and corrective action plans in one easy to use graphical environment.
Matrix Gemini LIMS, with its set of configuration tools can be configured to support R&D and QA/QC laboratory testing regimes to help ensure ongoing product quality and to help meet regulatory compliance needs such as in Good Manufacturing Practice. Raw materials and finished products can be tested against Master Record specifications and release mechanisms implemented for Batches and Lots. Defined workflows help ensure adherence to quality processes and full traceability of any actions carried out can be provided.
