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4-Hour Virtual Seminar on Qualification (IQ, OQ, PQ) and Validation of Laboratory Equipment and Systems for Regulated Industries (Pharma, Biotech, Devices, etc-)

5308
Duration : 4 Hours

Joy L. McElroy,

Upon earning a degree in Zoology at North Carolina State University, Joy began working in the pharmaceutical and biotech industries in 1992 at Pharmacia & UpJohn performing Environmental Monitoring and Sterility Testing.  Her work allowed her to move into a supervisory role at Abbott Labo 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

Get In Touch

Subject : 4-Hour Virtual Seminar on Qualification (IQ, OQ, PQ) and Validation of Laboratory Equipment and Systems for Regulated Industries (Pharma, Biotech, Devices, etc-)


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