LIMS has transformed the chemical laboratory in the area of data management by establishing a complete framework of efficient data handling. Advanced solutions automate workflows for enhancing data accuracy and the integrity of results.
FDA warning letters continue to highlight the issue of ensuring data integrity within laboratories. How are you ensuring data is not changed (deliberately or otherwise) and is stored securely?
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.
After 35 years in the Laboratory Informatics business Autoscribe Informatics have addressed multiple myths and misconceptions concerning laboratory information management systems (LIMS) and their implementation.
Implementing LIMS can be intimidating for most people. What if the cost doesn’t meet the expectation, what if the system fails, what if the work becomes too rigid and etc. There is always a risk in any business. However, take it as an investment is all about spotting potential and taking a calculated risk.
When laboratories start thinking about a laboratory information management system (LIMS) a common question they ask is ‘what is it going to cost?
As a tight labor market makes it difficult to find staff, and tougher economic conditions start to bite, laboratory managers are being forced to think hard about driving efficiency.
If your current LIMS is slowing down the laboratory turnaround times, becoming a burden to use, and demotivating staff, it’s time to upgrade!
Acceptable Quality Limit (AQL) sampling is used to determine whether an entire batch (or order) has met a client’s specification, based on a statistical sample of that batch.
LIMS Instrument Integration allows customer to have complete data integrity with ability to track & trace any analytical results for audit and/or historical purposes.
