GMP COMPLIANCE FOR REAL TIME PROCESS MONITORING, Q 2016 - How to Properly Monitor Process & Performance of Pharmaceutical Solid Dosage Equipment - By Compliance Global Inc

Website https://complianceglobal.us/product/700495/MichaelLevin/how-to-properly-monitor-process-performance- | Edit Freely

Category Education; E-Learning

Deadline: August 11, 2016 | Date: August 11, 2016

Venue/Country: Online Training, U.S.A

Updated: 2016-07-13 17:56:45 (GMT+9)

Call For Papers - CFP

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: supportcomplianceglobal.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.