QUMAS to launch latest version of QUMAS ComplianceSP™ on SharePoint 2010 at DIA 2012 Annual Meeting.
Cork, Ireland – June 21, 2012 - QUMAS, a leading provider of software solutions to the Life Sciences industry, announced today that it will be launching the latest version of QUMAS ComplianceSP™ at the upcoming 48th Annual Drug Information Association Conference being held at the PA Convention Centre in Philadelphia on June 25-27, 2012.
QUMAS ComplianceSP™ on SharePoint 2010 is an innovative document and process management solution for Regulatory Affairs, Quality Assurance and Compliance Management, combining the power of SharePoint 2010 with the proven regulatory domain expertise from QUMAS. Expert members of the QUMAS team will attend, participate in and speak at the DIA 2012 conference where they will discuss industry trends and also demonstrate the QUMAS Platform of Compliance and Quality Management solutions.
As well as launching the latest version of ComplianceSP, QUMAS will also provide opportunities for DIA conference attendees to avail of complimentary 30 minute Quality Management Assessments of their enterprise’s current Quality capabilities – these assessments will be carried out by expert QUMAS compliance consultants.
QUMAS will demonstrate how it is possible to choose a single quality management system for documents, deviations and CAPAs from one vendor, lowering the total cost of ownership, simplifying validation, and reducing maintenance costs and complexity. With their Quality Management Solution (QMS), QUMAS enables enterprises to implement a complete solution that addresses all quality management requirements from SOP management with built-in electronic signatures and audit trails, Deviation and CAPA management, providing real-time, usable dashboards that facilitate trend analysis and decision making.
As the number of consultation sessions available is limited, it is advisable to contact QUMAS in advance to schedule a free 30 minute session, by calling 800-577-1545, emailing firstname.lastname@example.org or alternatively visiting QUMAS at booth # 1143.
Warren Perry, GRCP, Compliance Consultant with QUMAS, will present the following session at the conference, “The Role of Corrective and Preventive Action (CAPA) in GCP/GLP Audit Quality Managements Systems: Deviation Management: SOPs and CAPAs for GCP, GLP and GMP” on Thursday, June 28, 2012 at 9:00am EDT.
All attendees who visit the QUMAS booth during the conference are eligible to enter a drawing for a chance to win one of 3 Amazon Kindle eReaders every day.
QUMAS is the leader in Compliance and Quality Management Solutions for the Life Sciences industry, with more than 260 global customer deployments and domain expertise in regulatory compliance since 1994.
QUMAS Quality Management solutions provide Electronic Document Management (SOPs, QA documents), Electronic Process Management (CAPA, Deviation, Change Control, Audit), and GMP Compliance Management. QUMAS Regulatory Affairs solutions provide content and Submission Management including eCTD authoring templates, collaborative review, full integration with leading publishing solutions, scanning, and automated import of paper documents.
The QUMAS Compliance Platform is available on Microsoft SharePoint 2010, Oracle, EMC Documentum and Microsoft SQL Server.