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Global Regulations for Equipment Qualification and Validation of Processes in the Pharma Manufacturing
Presented By ComplianceOnline
Wednesday, September 29th at 9:30am EST
Online sale ends: 09/29/21 at 8:30am EST
online event
6201 America Center Drive Suite 240 San Jose, CA 95002, USA
San Jose, CA 95002
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Description

Learning Objectives:

Upon completing this course participants should:

  • Understand what the global expectations are for equipment qualification and validation.
  • Understand the documents required for equipment qualification and process validation and how to manage documents appropriately.
  • Understand and know how to write and maintain a Validation Master Plan.
  • Write and execute sound protocols for equipment qualification (IQ, OQ, PQ) and process validation.
  • Qualify already existing systems and requalification
  • Be able to collect data, conduct tests, and obtain all necessary documents.
  • Understand the different types of validation.
  • Understand Performance Validation.
  • Know the guidelines on validating analytical methods and processes.
  • Support equipment qualification and validation through the quality management system, risk analysis, calibration and maintenance, and change control.
  • Understand and know the principles of auditing the equipment qualification and validation.
  • Understand external qualification and validation from a contract manufacturer, and qualification and validation by a supplier.
  • To investigate true root causes of problems and to evaluate and prioritize solutions
  • Problem solving methods to help you asses which is best for your situation
  • Develop successful implementation plans
  • Perform risk assessments effectively

Presented By

9:30am to 5:30pm
Doors open at 9:30am

Age
All Ages

online event<br> 6201 America Center Drive Suite 240 San Jose, CA 95002, USA<br> San Jose, 95002

18887172436

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