Medical device manufacturers are often tasked with documenting the process to comply with regulatory requirements and improving quality to adhere to customer specifications. Failure to do not just one, but all of the above is not an option in most medical device process scenarios. That's where capability analysis comes in. We invite to take a look of how to start today. (60 min).
In this webinar you will learn how to:
- Select the right analytical tools, how and when to use them from control charts to probability plots and goodness-of-fit test results to capability estimates such as Cp, Cpk, Pp, Ppk and sigma level.
- Use capability analysis to estimate the proportion of product that meets specifications and determine if that is acceptable for company and customer specifications, as well as regulatory requirements.
- Profile the outcome of a process using a tolerance interval.
