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.
3-Hour Virtual Seminar on Qualification (IQ, OQ, PQ) and Validation of Laboratory Equipment and Systems for Regulated Industries 2019 covers topics such as:
- 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
3-Hour Virtual Seminar on Qualification (IQ, OQ, PQ) and Validation of Laboratory Equipment and Systems for Regulated Industries 2019 is intended for:
- 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
