3-Hour Virtual Seminar on Qualification (IQ, OQ, PQ) and Validation of Laboratory Equipment and Systems for Regulated Industries 2019

  • 29 May 2019
  • Webinar

Description

3-Hour Virtual Seminar on Qualification (IQ, OQ, PQ) and Validation of Laboratory Equipment and Systems for Regulated Industries 2019 is a webinar dedicated to various phases of Qualification activities.

Topics
  • Quality Systems, Paradigm Shift, Global Perspectives
  • Introduction
  • Risk Assessment
  • QA/QC Validation
  • Regulatory and QS Requirements
  • Measurement, Resolution, Errors, and Uncertainty
  • USP chapter 1058
  • The Product Life Cycle Concept
  • Strategies for Validation
  • Examples of Various Systems
  • Training Requirements
  • Documentation /Master Validation Plan
  • Examples of Various Systems
Who should Attend
  • Managers
  • Scientists
  • Quality Assurance / Quality Control Staff
  • R&D Personnel
  • Validation Coordinators
  • Validation Managers
  • Regulatory/Compliance Managers
  • Production and Process Development Personnel
  • Technicians Study Directors(GLP)
  • Chemists
  • Pharmaceutical Development
  • Qualified Persons (EMEA)
  • CRO Managers, Accredited Laboratories in general
  • CRO Staff
  • Any one engaged with Test Methods

Past Events

Important

Please, check "3-Hour Virtual Seminar on Qualification (IQ, OQ, PQ) and Validation of Laboratory Equipment and Systems for Regulated Industries" official website for possible changes, before making any traveling arrangements

Event Categories

Government & Global Issues: Law & Regulations
Health & Medicine: Medical laboratories
Science: Laboratories

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