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FDA Compliant QC and QA Practices – Creating a Perfect, Audit-Ready QMS
This Webinar is over| Date | Aug 10, 2018 |
| Time | 03:00 PM EDT |
| Cost | $15070.00 |
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Online
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In the pharmaceutical world, the term “quality” has several definitions. Generally speaking, quality means the product is fit for its’ intended use, is free from defects, and meets or exceeds customer expectations. The general public assumes manufactured pharmaceutical products are safe, efficacious, and have the correct identity. The Quality Control and Quality Assurance units within our manufacturing facilities are responsible for ensuring pharmaceutical companies manufacture quality products. Within those functions, some common questions arise…
Areas Covered in the Session :
Who Should Attend:
Areas Covered in the Session :
- Discover FDA expectations for Quality Control and Quality Assurance
- Review the roles of Quality Control and Quality Assurance in your facility
- Learn how to avoid receiving 483s for Quality Control and Quality Assurance issues
- Identify the requirements for a Sound QMS
- Recognize how to implement and apply GMP concepts to your Quality Control and Quality Assurance roles
- Learn how to implement an effective audit ready QMS
Who Should Attend:
- Research and Development Departments
- Quality Control Departments
- Quality Assurance Departments
- Validation Professionals
- Management and Supervisory Personnel
- Regulatory Departments
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