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2020 - Pharmaceutical Manufacturing Equipment Qualification And Maintenance
Date2020-04-22
Deadline2020-04-22
VenueOnline Event, USA - United States 
KeywordsDesign qualification; Installation qualification; Operation qualification
Topics/Call fo Papers
The importance of risk management for manufacturing equipment
Validation Master Plans
Planning for new equipment, commissioning, and completing the design qualification
Installation Qualification
Operational Qualification
Performance Qualification
Process Validation
Planning for equipment maintenance
Documenting equipment maintenance
The connection with change control
When to revise your equipment maintenance plan
Validation Master Plans
Planning for new equipment, commissioning, and completing the design qualification
Installation Qualification
Operational Qualification
Performance Qualification
Process Validation
Planning for equipment maintenance
Documenting equipment maintenance
The connection with change control
When to revise your equipment maintenance plan
Other CFPs
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- HIPAA Breach Evaluation and Reporting - What Qualifies as a Reportable Breach and how to Report It
- How To Establish an Effective Chief Compliance Officer's (CCO) or Chief Risk Officer's (CRO) Function - Organization and Responsibilities
- Improving Case Management Discharge Planning
- Supplier and Service Provider Controls: FDA Expectations
Last modified: 2019-11-08 23:37:01