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

Event Description

Overview:

This webinar course covers a variety of topics on validation of pharmaceutical product and process according to FDA standards and others.

Why Should You Attend:

FDA Guidance on Process Validation: General Principles and Practices
Lifecycle and process validation
ICH Q10, FDA and EU – focus on validation
cGMP regulations and Process Validation Guidance
Data analysis and statistical tools for Process Quality Management (PQM)
Examples of statistical tools and ASTM standards
Process Verification vs. Process Validation

Areas Covered in this Webinar:

Qualification vs. validation vs. verification
Life Cycle approach to validation
Regulations for Process Validation: Review of FDA, GHTF, and GAMP Requirements
Documentation and testing: Installation Qualification (IQ), Operation Qualification (OQ) and Performance Qualification (PQ)
Acceptance Criteria of equipment qualification Process Validation
Validation Protocol as per FDA standards

Learning Objectives:

To acquire an in-depth understanding of modern process and equipment validation techniques

Who Will Benefit:

Formulators
Process Engineers
Validation/Regulatory Compliance/ Quality Assurance Personnel
Production Managers who want to make sure that their equipment and processes are in compliance with validation requirements of various regulatory bodies and directives

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:

http://bit.ly/28QOSnK

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

Fax: +1-516-900-5510

If the Life Cycle Process Validation According to FDA and other Standards - 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

Website: http://bit.ly/28QOSnK...
Conference/Event Dates: 07/21/2016 - 07/21/2016
Conference/Event Hours: 1:00
Classification: B2B
Primary Industry: Pharmaceutical
Other Industries: Clinical Pharmacology, Pharmaceutical, Professional Healthcare
Cost to Attend: Live Session for one participant Price: $175.00
Audience: Formulators
Process Engineers
Validation/Regulatory Compliance/ Quality Assurance Personnel
Production Managers who want to make sure that their equipment and processes are in compliance with validation requirements of various regulatory bodies and directives
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

Advance Networking

How do I show up here?
 
Mark Travers

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