Ensuring Closed Loop CAPA
Duration: 1 Hour
Corrective and Preventive Action (CAPA) is the core of a sound quality management system and is at the center of compliance programs for FDA regulations and ISO 9000 standard. Quality managers are finding that point-solutions and spreadsheet-based systems are inadequate for ensuring a closed-loop CAPA process. Companies are looking for ways to implement a systematic and consistent CAPA process to increase transparency and efficiency.
In this webinar, we will review common bottlenecks and productivity issues in CAPA management and demonstrate key capabilities of the MetricStream CAPA Management solution that address them.
- Accelerated CAPA investigation, approval, and closure with automated workflows
- Independent processes for containment, corrective, and preventive actions
- Improved communication and teamwork with parallel and sequential activities
- Real-time reports and dashboards for the CAPA process metrics and analytics
Panelists |
Ed Park
Director - FDA Compliance |
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Raghuraj Gaikwad
Manager - FDA Compliance |
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Register to View this Recorded Webinar
| For more information, please call (650) 620-2974 or email webinar@metricstream.com. |
