6-Hour Virtual Seminar on Qualification (IQ, OQ, PQ) and Validation of Laboratory Equipment and Systems for Regulated Industries (Pharma, Biotech, Devices) - Webinar - ResearchAndMarkets.com

DUBLIN--(BUSINESS WIRE)--The "6-Hour Virtual Seminar on Qualification (IQ, OQ, PQ) and Validation of Laboratory Equipment and Systems for Regulated Industries (Pharma, Biotech, Devices)" webinar has been added to ResearchAndMarkets.com's offering.

This webinar 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 the 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.

Key Topics Covered:

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

For more information about this webinar visit https://www.researchandmarkets.com/r/e7bwd1