Corrective and Preventive Action (CAPA) Process Planning for Clinical Research Professionals
Corrective and Preventive Action (CAPA) Process Planning for Clinical Research Professionals
To purchase access for your team, or if you have any questions, email us at info@clinicalpathwaysresearch.com.
Course outline HERE
INTERACTIVE DEMO AVAILABLE BELOW
Sponsors, 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 a CAPA process and how it links 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.
Course Length: 60 minutes
INCLUDES:
Unlimited access to the content for 45 days from your initial day of purchase.
Certificate of completion
Case Studies
Post-Assessment
Knowledge Checks
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.
AUDIENCE
All clinical research personnel
INTERACTIVE DEMO:
