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.
CAPA Simplified - A one-form, easy-to-complete, method for simplifying your CAPA Process 2019 covers topics such as:
- 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.
CAPA Simplified - A one-form, easy-to-complete, method for simplifying your CAPA Process 2019 intended for:
- Regulatory Affairs
- Quality assurance
- Managers
- Quality Control Directors
- Regulatory Compliance Directors