Compliance4All will organize a 3-hour webinar on “Statistical Process Control (SPC): A Detailed Introduction” on July 18

2024-04-08 04:27:44 Education

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Fremont, CA: Compliance4All, a leading provider of professional trainings for all the areas of regulatory compliance, will organize a webinar on the topic, “Statistical Process Control (SPC): A Detailed Introduction” on July 18. This webinar will be of three hours’ duration, and the expert is John N. Zorich, a very senior consultant for the medical devices industry. Please visit http://bit.ly/2tsb2DI to enroll for this webinar.

That organizations have an imperative to improve the quality of their standards is obvious and doesn’t need restating. Statistical Process Control is considered the most successful method for achieving product quality. In analyzing and correcting variations to the processes, it helps an organization that implements it have a more than reasonable chance of ensuring quality of standards with a relatively low cost on its endeavor.

Understanding Statistical Process Control and its manifold uses
Statistical Process Control is a statistical tool that, with the help of some Quality Indicator inputs, objectively identifies when it is worthwhile to perform a formal investigation of manufacturing variation with the intention of identifying and reducing its cause. SPC intuitively and continually calibrates its sensitivity to ensure that such investigations are carried out only when there is a reasonable chance of identifying causes of variation. The efficiency of the SPC can be gauged from the fact that the information it throws up can be used to calculate the percentage of items that are within the specification limits.

SPC can also be used to:
o Meet the ISO’s requirements for continual improvement;
o Meet the FDA’s requirements on control and monitor production processes;
o Monitor complaint rates
o Determine if there has been what is termed a “significant” increase in complaints, which would invite a vigilance report from the MDD and/or an FDA MDR submission.

These aspects of the SPC will be explained in detail over three hours at this webinar. The aim of this 180-minute webinar is to offer strategies for designing process control and operator activities aimed at:
o Reducing variation
o Adjust for variation during manufacturing
o Reducing the possibility for operator error.

José will explain all these at this webinar while covering these areas:
o Definition of relevant terms
o Types of control charts
o Calculation of control limits for XbarR, XbarS, XmR, P, nP, and U-charts
o Rules for detecting "out of control"
o Sampling issues
o Auto-correlation and rational subgrouping
o Sample Size issues
o Process Capability Indices: Cp, Cpk, Pp, Ppk (calculation, choice, interpretation, confidence limits, & calculation of %-in-specification of off-center processes)
o Non-normal data effects on SPC charts and on Capability Indices
o SPC Program implementation.

The learning offered at this webinar is valuable for professionals holding the designations of QA/QC Supervisor, Process Engineer, Manufacturing Engineer, QA/QC Technician and Manufacturing Technician.