Statistical Concepts of Process Validation - Webinar By GlobalCompliancePanel

Why you should attend:
If you conduct process validation, you need to ensure that your results are valid. Beyond the regulatory requirements, statistical approaches will help you achieve the desired result - processes that produce only conforming material. This is the essence of the statistical approach. This webinar presents the statistical approach that will help you validate your processes. Your team should attend this webinar if you cannot easily answer these questions.

Can you give the statistical rational for you verification sampling plans? Can you state the desired and actual process capability you need to achieve? Can you list the worst-case input parameter combination for your process? Do you know how to determine challenge points for your process? Have you set action limits for your process inputs?

Areas Covered In the Seminar:

QMS Requirements for Process Validation FDA’s QSR (21 CFR §820.75) ISO 13485:2003 The Statistical Process Model Relating input to output The Process Output Sampling Inspection Process Capability The Process Input Parameters Design of Experiments The Challenge Points Risk Management Production Information Validated Processes as High Risk

Who will benefit: People in the following roles can especially benefit from the knowledge in this webinar:

Quality Managers Quality Engineers Production Managers Production Supervisors Manufacturing Engineers Production Engineers Design Engineers Process Owners

 

Price List: Live : $245.00 Corporate live : $995.00 Recorded : $295.00   webinars@globalcompliancepanel.com http://www.globalcompliancepanel.com   Phone: 800-447-9407 Fax: 302-288-6884