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Process Validation Requirements & Compliance Strategies

 
  May 28, 2018  
     
 
NetZealous LLC, DBA compliance4All, Online Event
2018-07-17



Overview:

This Process Validation Requirements webinar will review process validation basics, with emphasis on looking beyond compliance towards achieving a robust process. Review of process validation basics, with emphasis on looking beyond compliance towards achieving a robust process.

Why should you Attend: When used as intended, process validation can provide increased process reliability, improved yields, and reduced operating expenses.

Areas Covered in the Session:

  • Global Harmonization Task Force requirements (includes FDA and ISO)
  • Installation Qualification (IQ)
  • Operational Qualification (OQ)
  • Performance Qualification (PQ)
  • Design Qualification
  • Facilities and utilities
  • Strategies for achieving a robust and reliable process
  • Typical process validation protocols

Who Will Benefit: Managers, Supervisors, Directors, and Vice-Presidents in the areas of:
  • Research & Development
  • Quality Engineers and Auditors
  • Manufacturing Engineers
  • Quality Assurance & Quality Control Teams
  • Operations Teams
  • Document Control
  • Device Development Teams
  • Personnel involved in Verification and Validation Planning, Execution and Documentation for Devices

 
 
Organized by: Compliance4All
Invited Speakers: Jose Mora is a Principal Consultant specializing in Manufacturing Engineering and Quality Systems. For over 30 years he has worked in the medical device industry specializing in manufacturing, process development, tooling, and quality systems.
 
Deadline for Abstracts: 2018-07-17
 
Registration: Cost : $150.00
Event link :    http://www.compliance4all.com/control/w_product/~product_id=501950LIVE/~sel=LIVE/?channel=hum-molgen-july_2018_SEO
Contact Details:
NetZealous LLC, DBA compliance4All    
Phone: +1-800-447-9407
Email: support@compliance4All.com
E-mail: compliance4all14@gmail.com
 
   
 
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