A famous sports coach once said: “If you are not keeping score, you are just practicing.” The FDA’s Quality System regulation says that manufacturers “shall establish and maintain procedures for… verifying the acceptability of process capability and product characteristics.” Folks, that’s asking you to keep score. But regulatory compliance is not the only issue. Any organization that wants to pursue world-class quality should rely on meaningful measures of quality.
The primary goal of this webinar is to develop a simple flow chart on methods to establish and maintain product and process capability through meaningful measures of quality. Statistically valid techniques and industry best-practices are presented. FDA regulatory requirements and the recommendations of the guidance documents developed by the FDA and the Global Harmonization Task Force (GHTF) will be discussed. Best practices applied in a wide variety of industry settings will be illustrated.
For registration information: https://us-tdm-tso-15eb63ff4c6-1626e-169df4b0a12.force.com/s/lt-event?id=a1Y2E000009UKYC