The Path To An Intelligent Quality Management System

Requirements
  • GEO: USA and Canada
  • Company Size: 50+ Employees
  • Industries: Pharmaceuticals, Biotech, Medical Device except Diagnostic Substances, Surgical and Medical Instruments and Apparatus
  • Titles: IT, Engineering, Operations, Analytics, Process, Compliance, Quality System Admins, Quality Control Manager, Quality Systems leaders, Quality Engineer, Quality Assurance
  • Job Level: Manager +
Overview

Over 53% of quality management professionals say digitization is the highest priority in their company. To meet the demands of an evolving regulatory and competitive landscape, pharmaceutical, medical device, biopharmaceutical, and biotechnology companies must digitize their quality management system (QMS) and take efficiency and data connectivity to new heights.

By digitizing you can automate and manage all your critical compliance, training, and quality event documents throughout the product life cycle. You’ll have new tools and business intelligence to increase profitability and drive business excellence.

Top reasons our community cites for adopting or considering this solution:

  • Legacy Systems: Current systems not designed for today’s business/operations requirements.
  • Slow Cycles: Document approval/sign-off cycles can average 30 days or more.
  • Data Management: Too much time spent collecting/aggregating/structuring data.
  • ​​​​​​​​​​​​​​Death by CAPA: Too many wrongly diagnosed CAPAs that waste time and clog up system.
  • Inefficient Training: Difficulty in managing and tracking the training status of every employee.
  • Human Errors: Inconsistency in process and gaps in systems let errors persist.
  • Poor Analytics: Quality data is siloed and is time intensive to aggregate and analyze.
  • ​​​​​​​​​​​​​​Operational Visibility: Lack of real-time view of quality operations across organization.

You must be directly involved in your company’s evaluation process for solutions like this, or in the management chain for people who do. You must be a hands-on user of the prospective solution or in the management chain of users. Please do not register for programs that are an unlikely fit. Your credibility and ours depend on it.

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