CAPA Simplified - A one-form, easy-to-complete, method for simplifying your CAPA Process 2019

CAPA Simplified - A one-form, easy-to-complete, method for simplifying your CAPA Process 2019 is a webinar dedicated to "Learn 21 CFR subpart J of FDA regulations related to CAPA, how to integrate CAPA with other branches of QMS.

Topics

• Responsibilities of manufacturers
• Get an in-depth understanding of what regulatory agencies such as the FDA are requiring for CAPA.
• Documentation requirements
• Evaluate your already-existing CAPA process to determine if it meets requirements.
• Overview of commonly-used root cause analysis functions.
• Determine if your CAPA system is robust enough to ensure actions are effective or overly-complicated and preventing smooth operation.
• Tips and tricks for implementing a successful CAPA system.
• Understand some misconceptions with CAPA implementation.

Who should Attend

• Regulatory Affairs
• Quality assurance
• Managers
• Quality Control Directors
• Regulatory Compliance Directors