Does your Equipment Program Meet Current Regulatory Expectations - Webinar By GlobalCompliancePanel

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Why you should attend: The equipment Program is a critical component of both GMP and GLP laboratories. It contributes to the quality and therefore reliability of the generated data which is required for critical for go-no-go decisions. An effective Equipment Program is also an expectation in GLP and GMP laboratories.

Areas Covered In the Seminar:
FDA requirement for Equipment systems
Overview of GMP/GLP requirements for equipment
IIQ/OQ/PQ of Equipment
Equipment database
Equipment SOPs
Equipment Calibration and maintenance
Review of equipment related citations in recent Warning Letters
Who will benefit: This course is intended to provide training how to perform OOS/OOT investigations
QC Supervisors and Management
QA personnel
QA Management
Documentation management specialists
Regulatory affairs personnel