4-Hour Virtual Seminar on Qualification (IQ, OQ, PQ) and Validation of Laboratory Equipment and Systems for Regulated Industries (Pharma, Biotech, Devices, etc-)
Duration : 4 Hours
Joy L. McElroy,
Joy McElroy entered the pharmaceutical industry in 1992 shortly after earning a Bachelor of Science degree at North Carolina State University. She began at Pharmacia & UpJohn performing environmental monitoring and sterility testing. From there she moved into a supervisory role at Abbott Labor Read more
This seminar will aim at understanding and scoping out various phases of Qualification activities that will be integrated with the perspectives of Instrument Control, System Suitability Test (SST), Analytical Methods Validation and ensuring Data Integrity for Regulatory Compliance.
Why you should Attend:
This is an area of growing concern, sometimes ridden with uncertainty as to what needs to be done at each of stages of the Product Lifecycle. In modern Pharmaceutical and Biotech laboratories, a composite array of various gadgets, devices, analytical instruments and computerized systems are used daily.
Agenda:
Session 1
• Introduction
• Quality Systems, Paradigm Shift, Global Perspectives
• QA/QC Validation
• Risk Assessment
Session 2
• Measurement, Resolution, Errors, and Uncertainty
• Regulatory and QS Requirements
• The Product Life Cycle Concept
• USP chapter 1058
• Examples of Various Systems
Session 3
• Strategies for Validation
• Documentation /Master Validation Plan
Session 4
• Training Requirements
• Examples of Various Systems
What You Get:
• Training Materials
• Live Q&A Session with our Expert
• Participation Certificate
• Access to Signup Community (Optional)
• Reward Points
Who Will Benefit:
• Scientists
• Managers
• R& D Personnel
• Quality Assurance / Quality Control Staff
• Validation Managers
• Validation Coordinators
• Production and Process Development Personnel
• Regulatory/Compliance Managers
• Chemists
• Technicians Study Directors(GLP)
• Qualified Persons (EMEA)
• Pharmaceutical Development
• CRO Staff
• CRO Managers, Accredited Laboratories in general
• Any one engaged with Test Methods
Please reach us at 1-888-844-8963 for any further assistance or if you wish to register
100% MONEY BACK GUARANTEED
Refund / Cancellation policyGet In Touch
Similar Trainings
The Most Common Problems in FDA Software Validation & Verification
LIVE : Scheduled on
09-July-2025 :01:00 PM EDT
|
