LIMS Ensures FDA 21 CFR Part 11 Compliance
LIMS helps laboratories comply to FDA 21 CFR Part 11 by enforcing signature policies for all electronic records. Ensuring electronic records and electronic signatures can be relied upon in the same way as paper records and handwritten signatures.
The global pharmaceuticals market is worth over $750 billion a year, a figure that is expected to continue to rise. In a highly competitive and increasingly expensive market place it is important that cost efficiencies are maximized, while meeting all critical compliance requirements.
The Food Standards Modernization Act (FSMA) is driving producers towards LIMS & BIMS solutions.
Pittcon 2019 sees the latest version of Matrix Gemini LIMS (Laboratory Information Management System) from Autoscribe Informatics. Showcasing Matrix Instrument Data Acquisition System (MIDAS) and other new features.
Discover the benefits of implementing LIMS and BIMS solutions into food testing laboratories in today's FDA regulated food manufacturing environments.
Meeting industry standard can be an imperative for many laboratories. Working to these requisite standards is not necessarily a guarantee of product safety. There are clear deifinitions of how to achieve standard 100 registration, but it's a more collaborative approach that benefits the entire supply chain.
Efficient management of the laboratory process helps to keep costs down and improve service levels. Laboratory information management systems (LIMS) can improve management of the entire process.







