Corrective and Preventive Action (CAPA) - Process of the Quality Management

OVERVIEW Corrective and preventive action (CAPA) is a process of the quality management system which, like other processes, has suppliers (other processes of the QMS), inputs such as corrective action requests and audit findings, a series of clearly defined activities, outputs, and customers.
WHY SHOULD YOU ATTEND
Corrective and preventive action (CAPA) is likely to be the most important process of any quality management system (QMS) because so many other activities depend on it. These include not just the traditional processes for handling poor quality, customer complaints, and audit findings but also outputs of the management review meeting and stakeholder-identified risks and opportunities.
AREAS COVERED
1. Supplier and customer processes of CAPA; the numerous processes of the quality management system that supply inputs and receive outputs from CAPA.
2. CAPA is a leading source of ISO 9001 and IATF 16949 findings, and FDA audit 483 observations.
LEARNING OBJECTIVES
The webinar will provide a comprehensive overview of formal corrective and preventive action (CAPA) and also a much simpler process for issues that can be resolved by a process owner on the factory floor. Both processes are applicable not only to poor quality but also occupational health and safety (OH&S) and the other six Toyota production system wastes (muda).
WHO WILL BENEFIT
ISO 9001:2015 and IATF 16949 users, including but not limited to manufacturing and quality managers, engineers, and technicians.
Use Promo Code MDTD20 and get flat 20% discount on all purchases.
To Register (or) for more details please click on this below link:
https://bit.ly/2Xl2FtE
Email: [email protected]
Toll Free: +1-888-300-8494
Tel: +1-720-996-1616
Fax: +1-888-909-1882

Read More

View Less