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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
- 7th International Conference and Exhibition on Pharmaceutical Development and Technology
- International Conference on Pharmaceutical Microbiology
- The 7th International Conference on Metal Material Processes and Manufacturing
- The 4th Global Congress on Pharmaceutical Sciences and Clinical Research （PSCR2025）
- 9th International Conference on Advanced Manufacturing and Materials(ICAMM 2025)
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
- Hospital Case Management Rules and Regulations: Doing it Right
- 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