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2020 - Pharmaceutical Manufacturing Equipment Qualification And Maintenance

Date2020-04-22

Deadline2020-04-22

VenueOnline Event, USA - United States USA - United States

KeywordsDesign qualification; Installation qualification; Operation qualification

Websitehttps://www.complianceonline.com/pharmac...

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

Other CFPs

  1. Hospital Case Management Rules and Regulations: Doing it Right
  2. HIPAA Breach Evaluation and Reporting - What Qualifies as a Reportable Breach and how to Report It
  3. How To Establish an Effective Chief Compliance Officer's (CCO) or Chief Risk Officer's (CRO) Function - Organization and Responsibilities

Last modified: 2019-11-08 23:37:01