Product category:
Laboratory information management system (LIMS)
News Release from: Autoscribe | Subject: Matrix Stability system
Edited by the Laboratorytalk Editorial
Team on 17 October 2007
Lims stability study module for
pharmaceutical QA
Partnership provides a comprehensive protocol design, management and compliant lab procedure execution platform for stability studies in a multi-site pharmaceutical quality operation
VelQuest and Autoscribe announce an integration partnership to support a major multi-site pharmaceutical company The company is implementing the VelQuest SmartLab GMP electronic notebook system for QC/QA cGMP laboratory execution, instrument integration and data capture with integration directly to SAP
This article was originally published on Laboratorytalk on 10 Jun 2008 at 8.00am (UK)
Related stories
Track-IT handles all your sample tracking needs
Today, companies and organisations operate in a much more complex environment as far as tracking and reporting on events, activities or items as they occur
Using the web to manage ISO 17025 calibration
Calibration Technology, Ireland (CTL) works with laboratories to help them optimise the accuracy of their test results by ensuring that their pipettes are precise
To comprehensively design protocols and manage stability data, VelQuest and the client's choice is the Matrix Stability system, developed by Autoscribe, and supplied in the USA by Zumatrix.
"The Matrix Stability system was designed in cooperation with several pharmaceutical companies and our US distributor, Zumatrix", says John Boother, managing director of Autoscribe.
"At our joint client's multi-site quality organisation, VelQuest's SmartLab platform and the Matrix Stability system combine best-of-breed method execution, data capture and stability protocol design and data management for cGMP operations".
"A major goal in many companies is to eliminate the routine, non-value added and error-prone tasks through automation", said Ken Rapp, president and CEO of VelQuest.
"A key issue in the pharmaceutical industry is that a significant amount of people are dedicated to regulatory compliance functions that use costly paper-based processes.
"The SmartLab software has been deployed in cGMP facilities worldwide.
"Users have reported their ability to eliminate the paper-based data capture and documentation processes creating annual operational benefits yielding millions of dollars in efficiency gains.
"The integration of the Matrix Stability study system with SmartLab provides a comprehensive protocol design, method execution, automated data capture and compliant documentation management capability for this critical process in cGMP quality operations". Request a free brochure from Autoscribe ...
• Autoscribe: contact details and other news
• Email this article to a colleague
• Register for the free Laboratorytalk email newsletter
• Laboratorytalk Home Page
Search the Pro-Talk network of sites
