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Event

 
  September 18, 2018  
     
 
Compliancetrainingpanel, Online
2018-09-25


Description :
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 ?
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:
  • 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
About Speaker:
José Mora is a Principal Consultant and Project Manager specializing in Manufacturing Engineering, Quality Systems, and Lean Transformations. José is a recognized subject matter expert in process validation, lean manufacturing, lean controlled document systems, startup operations, process development and quality systems, having lectured internationally and presented webinars on these subjects.For over 30 years he has worked in the life sciences in positions ranging from Senior Engineer and Project Manager to Vice-President, specializing in manufacturing, process development, tooling, and quality systems. His medical device experience includes surgical instruments, PTA & PTCA dilatation and guiding catheters, plastic surgery implants and tissue expanders, urology implants and devices for the treatment of incontinence, delivery systems for brachytherapy, orthopaedic implants and instruments, and vascular surgery grafts and textiles.
 
 
Organized by: Compliance Training Panel
Invited Speakers: Process Validation Requirements & Compliance Strategies
 
Deadline for Abstracts: 2018-09-25
 
Registration:
Venue:Online
Speaker Name: Jose Mora
Price : $ 239
Tuesday, September 25, 2018
EST 13:00
Duration : 90 Minutes
Tel: +1-844-216-5230
Email:support@compliancetrainingpanel.com
https://www.compliancetrainingpanel.com/Webinar/Topic?WB=MP00110 
E-mail: event@compliancetrainingpanel.com
 
   
 
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