For an organization to move to and thrive in a culture of quality involves having consistent, reliable, robust business processes and data that promote continual improvement and deliver on quality objectives. This webinar considers some of the most important aspect of quality management, including techniques to achieve a modern maturity model (QMM). We discuss potential areas of improvement, such as a patient-centricity focus, the accuracy and completeness of data, and how to meet current and future regulatory requirements.
- Develop processes, products, systems with the patient in mind
- Rapidly respond to patient feedback
Integrated data management strategy including a fully electronic quality management system (QMS)
- Efficiency through data integration
- Effective signal detection and response
Strong regulatory intelligence to support oversight responsibilities
- Cost reduction through robust data gathering
- Proactive preparation for impending regulatory changes
Who should participate:
Drug manufacturing, pharmaceutical manufacturing, biologics organizations, medical devices; Job function: quality assurance (QA), quality control (QC), operations managers, quality management, pharmaceutical quality directors, MHA, MPH.
Though this course is being made available on USP’s Education site, the course content was developed by Pharmatech Associates, a USP company. USP has not independently reviewed or verified the accuracy of the course content.