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

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

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08/11/2016 - 08/11/2016

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Add to Your Calendar 08-11-2016 00:00:00 08-11-2016 00:00:00 11 How to Properly Monitor Process & Performance of Pharmaceutical Solid Dosage Equipment - By Compliance Global Inc. 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... true MM/DD/YYYY

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Compliance Global Inc
2754 80th Avenue
New Hyde Park, NY 11040
(516) 900-5515

Compliance Global Inc
(516) 900-5515

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

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Event Details

Website: https://complianceglobal.us/product/700495...
Conference/Event Dates: 08/11/2016 - 08/11/2016
Conference/Event Hours: 1:00
Classification: B2B
Primary Industry: Clinical Pharmacology
Other Industries: Clinical Pharmacology, Professional Healthcare
Cost to Attend: Live Session for one participant Price: $175.00
Audience: Formulators
Process Engineers
Validation Specialists
Quality Assurance Personnel
Production Managers occupied with Process and Product Quality Assurance
Show Owner:Compliance Global Inc.
Sponsorship: Yes
Sponsorship Details: Compliance Global Inc.

Booth Details

Booth Size Booth Cost   Available Amenities
No Exhibiting   Electricity: n/a
  Water: n/a
  Generator: n/a
  Marketing Vehicles Allowed: n/a
Other Booth Sizes Available: n/a

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