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EVENT DATE
Aug 2016
M T W T F S S
08091011121314
EXPO DATE
Aug 2016
M T W T F S S
08091011121314

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Online Event
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Type: Online Event

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

B2B

EVENT DESCRIPTION

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

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.

For more detail please click on this below link:

https://complianceglobal.us/product/700495

Email: referrals@complianceglobal.us
Toll Free: +1-844-746-4244
Tel: +1-516-900-5515

Fax: +1-516-900-5510

If the How to Properly Monitor Process & Performance of Pharmaceutical Solid Dosage Equipment - By Compliance Global Inc. is important to your business, act now and make the appropriate connections. See the contact information below.

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EVENT DETAILS

Primary Industry:
Clinical Pharmacology
Other Industries:
Clinical Pharmacology, Professional Healthcare
Audience:
Formulators
Process Engineers
Validation Specialists
Quality Assurance Personnel
Production Managers occupied with Process and Product Quality Assurance
Notes:
Show Owner:
Compliance Global Inc.
Sponsorship: Yes

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Show Owner
Compliance Global Inc.

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