QUMAS Quality Management Solution for Global Regulatory Compliance

Webinar description

  • Are you using separate point solutions for document management, deviation management, CAPA, change control, audits, learning management and reporting
  • Do you want to reduce maintenance costs and training overheads, provide more automation and synchronized compliance to your enterprise?

The QUMAS QMS is an industry leading solution for regulatory, quality and compliance management, and is live in production across tier 1 and 2 in the life sciences sector.

Learning Objectives

Download this webinar to learn about the core components of a fully compliant QMS solution, that can deliver business efficiencies as well as regulatory control. This webinar will focus on:

  • SOP Management – Document creation, editing, review and approval in conjunction with 21 CFR Part 11 compliance
  • Training Management – full learning management capabilities, read and understood, multiple choice examination, and electronic signature
  • Overview of CAPA, Deviation, Change Control, Audit, Complaints, others
  • Reporting and dashboards – getting the metric/analytics from the system in a timely manner

Featured Speaker

Cyril Walsh, BIOVIA, Senior Solutions Consultant

Duration: 59 mins

Originally aired: