Medical Devices 2011 - CAPA Details, Implementation and Q&A in Medical Device Setting

This 2-hr Medical Device CAPA training will cover key CAPA process skills such as identifying non-conformances, root cause analysis, and steps to implement CAPA and check its effectiveness in a Medical Device setting.

Why Should You Attend:

This webinar is tuned to address CAPA implementation in medical device manufacturing facilities. This CAPA training will instruct participants in the following key process skills:

Issue Review - Identify and prioritize non-conformances based on risk.
Root Cause Analysis - Investigate systemic issues for underlying cause.
Implementation & Effectiveness Checking - Solution selection, verify and validate, implement, monitor and confirm success.

Who Will Benefit:

This CAPA training is appropriate for individuals in medical device companies, and their suppliers, who are regularly called upon to resolve problems, or whose input would aid in preventing problems. Those who will benefir most include:

- Manufacturing Supervisors

- Engineers

- Product Managers

- Investigators

- Laboratory Managers

- QA/QC

- Regulatory Affairs

NOTE : Use this Promocode (128600) to avail 10% discount, valid upto 3rd December 2011.