OVERVIEW

Implementing a Quality Management System is organized by ComplianceOnline and will be held on Oct 27, 2021.

Who Will Benefit:
• Senior Managers, Managers & Supervisors
• Process Owners
• Departmental Heads
• Quality System, QA, QC and Continuous Improvement Managers and Personnel
• Quality Consultants
• Regulatory and Compliance Managers
• Change Control/Documentation Staff

Why Should You Attend:
Medicine quality requires meeting regulations and established specifications. Quality management in pharmaceutical industries is an important subject because the products are delivered directly into the consumers body, thus identity, purity safety and ultimately appropriate quality of product are critical. Ultimately the quality of pharma products is a legal issue and must be maintained in pharmaceutical products. In today’s highly regulated and competitive environment, with many existing drugs coming off patent and delivery to market slowing, companies often forget about quality processes.

Description:
This GLP quality system webinar provides a general overview of the Proposed Rule, a GLP QMS and its implementation, GAP analysis, Plan-Do-Check-Act cycle, process control and optimization theory and quality audits are utilized for the analysis of an existing QMS and the potential benefits, barriers steps to implementing an optimized GLP QMS.

Areas Covered in the Webinar:
• GLP Regulations
• Quality Management System (QMS)
? Definition
? Principles
? Purpose
? Function
? Elements
• Quality Policy
• Quality Objectives
• Quality Manual
• GLP SOPs
• Plan, Do, Check, Act Cycle
• GAP Analysis
• QMS Implementation Steps
• Process Control and Optimization Theory
• Process Criteria
• Quality Audit