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Pharmaceutical Quality Systems – 2018 Workshop
This Webinar is over| Date | Oct 4, 2018 |
| Time | 10:00 PM EDT |
| Cost | $24000 |
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Online
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Manufacturers in the pharmaceutical industry are always working to balance the demands of meeting global regulations and production costs, in an effort to produce the most innovative research and development while also producing safe, reliable prescription drugs. This workshop can help your company employ quality initiatives and quality control methodologies in order to ensure compliance of government guidelines, improve shrinking margins and help you win recognition as an industry leader.
Why You Should Attend:
This workshop will help you to develop practical cost effective quality management systems through this training course for pharmaceutical industries to implement effective QMS. We know how important it is to integrate regulatory, market and customer requirements for your complete product range into a streamlined Quality Management System (QMS). Our aim is to help you protect patient health and protect your business from regulatory and commercial risk by Practical Training of quality management systems.
Areas Covered in the Seminar:
Who Should Attend :
Professionals from Finished Pharmaceuticals, Biotechnology Products, Active Pharmaceutical Ingredients (API), and combination products organizations. A must attend seminar for Teams from:
Why You Should Attend:
This workshop will help you to develop practical cost effective quality management systems through this training course for pharmaceutical industries to implement effective QMS. We know how important it is to integrate regulatory, market and customer requirements for your complete product range into a streamlined Quality Management System (QMS). Our aim is to help you protect patient health and protect your business from regulatory and commercial risk by Practical Training of quality management systems.
Areas Covered in the Seminar:
- Pharmaceutical Quality Systems in GMP
- Regulatory Requirements
- PQS Elements
- Effective Handling of Deviations
- Change Control Management
- Laboratory PQS Compliance
- Failure Investigations
- Root Cause Analysis and CAPA Investigations
- Annual Product Quality Review
- Handling Complaints and Recalls
- Quality Risk Management
- Quality Metrics
- Case Studies and Practical Sessions
Who Should Attend :
Professionals from Finished Pharmaceuticals, Biotechnology Products, Active Pharmaceutical Ingredients (API), and combination products organizations. A must attend seminar for Teams from:
- Quality Assurance Departments
- Quality Control Departments
- Production Departments
- Manufacturing Departments
- Operations Departments
- Regulatory Affairs Departments
- Engineering Departments
- Documentation Departments
- Facilities Departments
- Warehousing Departments
- Laboratory Staff
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