Streamline Quality Metrics Through Innovative Technology

Register for this FREE webinar below:


With FDA finalizing its quality metrics guidelines, manufacturers are eager to understand what its expectations will be.  Once defined, companies need to ensure they are collecting those data points across all manufacturing sites and from multiple systems.

Criteria for technology solutions should include the ability to integrate with other key systems to collect required data, populate reports and electronic submissions to FDA.  Your company will need to make significant changes to or adopt new processes, procedures, personnel and IT/IS tools.

Join us on May 11th for a FREE webinar that will show you how to use innovative technology to streamline your quality metrics initiative.

You will learn:

  • How metrics fit into the overall vision on quality programs

  • How to implement the required quality metrics with internal company data used to monitor quality systems

  • What tools are available to capture and measure quality information from manufacturing sites, CROs and suppliers

If you are looking to implement a reporting framework that produces reliable, useful data that meets the FDA requirements, register today.


Who Should Attend

  • Auditors
  • Compliance officers
  • Consultants/service providers
  • Data management and statistics personnel
  • Executive management
  • General/corporate counsel
  • Investigators
  • Managers
  • Manufacturing directors and supervisors
  • Personnel new to the industry
  • Pharmaceutical and cGMP auditors
  • QA/QC personnel
  • Risk management specialists
  • Training personnel