How to Create an Effective Quality Management Plan
Learn how to create an effective Quality Management Plan (QMP) with key components, roles, execution steps, and continuous improvement strategies to ensure project success.
FDA Continues to Highlight Data Integrity as a QC Lab Issue
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?
Lab Indonesia Exhibition 2024
PT Agriya Analitika is back at Lab Indonesia 2024.
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.
LIMS Myths – Debunked
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.
Seminar: Reducing Business Risk with LIMS
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.
What is the cost of a LIMS?
When laboratories start thinking about a laboratory information management system (LIMS) a common question they ask is ‘what is it going to cost?
