6/04/2020
Why Take a Course in CAPA Process Planning?
Sponsor, CROs, and research sites are required by regulatory authorities and GCP to have an effective process to manage significant noncompliance through corrective and preventive action (CAPA) plans. These stakeholders should have procedures to support their CAPA system and documentation. Team members must understand the concepts and best practices of a CAPA process and how it should link into quality risk management.
This training is designed to provide this understanding and is an essential companion to training on a company specific CAPA system. It is also a foundation for the CAPA process and supports understanding through GCP industry specific case scenarios and other application exercises in each section.
Learning objectives:
Recognize why corrective and preventive actions are essential in maintaining quality in a clinical trial.
Apply the steps of the CAPA process in clinical trial scenarios.
Discuss challenges in performing CAPA activities and review potential solutions.
To sample an interactive demo or to purchase the full course, visit our store by clicking here.
Tired of training that goes on and on without understanding your needs? Clinical Pathways’ eLearning uses real-life case scenarios within a series of short lessons to help you recognize how the training applies to your day-to-day.
Interested in more than one course or to build a curriculum for your team? Clinical Pathways also offers convenient course bundles at a discounted rate. Each course comes with a certificate of completion as evidence of your training for audit readiness.
Need to train your entire department? Clinical Pathways offers enterprise solutions that are scalable to your department needs, including white label solutions or creation of customized or new content for your internal training. The deployment of the training can be through Clinical Pathways’ learning portal or through your company learning management system.
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