How to Properly Monitor Process & Performance of Pharmaceutical Solid Dosage Equipment - By Compliance Global Inc

11 August 2016 01:00-02:00, United Kingdom


Introduction
Overview:

This webinar covers topics on Process real time monitoring and quality control tools.

Why Should You Attend:

You will learn about regulatory guidance and requirements designed to improve real-time process monitor and control, as well as technical aspects of various instrumentation techniques. No special technical background is required.

Areas Covered in this Webinar:

Data-driven fault diagnosis and process monitoring methods
Code of Federal Regulations Title 21
Monitoring and control of process parameters and component and device characteristics during production
Pharmaceutical industry basic unit operations
Quality by Design (QbD) and modern process monitoring systems
Process and endpoint monitoring and control tools
Current GMP compliance practices and Risk-based PAT framework

Learning Objectives:

What can be monitored in mixing operations
What can be monitored in wet granulation operations
What can be monitored in dry granulation operations
What can be monitored in compaction operations
What can be monitored in coating operations
PAT Guidance and process monitoring devices
Monitoring for real-time quality management
FDA guidance and methodologies for risk-based monitoring

Who Will Benefit:

Formulators
Process Engineers
Validation Specialists 
Quality Assurance Personnel
Production Managers occupied with Process and Product Quality Assurance

For more information, please visit : https://complianceglobal.us/product/700495/MichaelLevin/how-to-properly-monitor-process-performance-of-pharmaceutical-solid-dosage-equipment/1
Email: support@complianceglobal.us 
Toll Free: +1-844-746-4244
Tel: +1-516-900-5515


Level: 
Intermediate

Speaker Profile:

Michael Levin, Ph.D., has edited a very popular “Pharmaceutical Process Scale-Up” handbook (3rd edition published in 2011), and has contributed chapters on “Tablet Press Instrumentation” and “Wet Granulation: End-Point Determination and Scale-Up” in the Encyclopedia of Pharmaceutical Technology. He also wrote dozens of validation protocols executed for various computerized systems and unit operations.
Speakers
Venue

United Kingdom

Organised by
Compliance Global Inc
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