Process Validation Requirements & Compliance Strategies

6 years ago Posted By : User Ref No: WURUR25462 0
  • Image
  • TypeWebinar
  • Image
  • Location Washington, Maryland, United States
  • Price
  • Date 25-09-2018
Process Validation Requirements & Compliance Strategies, Washington, Maryland, United States
Webinar Title
Process Validation Requirements & Compliance Strategies
Event Type
Webinar
Webinar Date
25-09-2018
Last Date for Applying
25-09-2018
Location
Washington, Maryland, United States
Organization Name / Organize By
Compliancetrainingpanel
Organizing/Related Departments
R&D
Organization Type
Event Management Company
WebinarCategory
Technical
WebinarLevel
International
Related Industries

Education/Teaching/Training/Development

Communications

Location
Washington, Maryland, United States

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.
  • 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:Jose 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.

Others Details

Venue:Online Speaker Name: Jose Mora Price : $ 239 Tuesday, September 25, 2018 EST 13:00 Duration : 90 Minutes Tel: +1-844-216-5230 Email:[email protected]

Registration Fees
Available
Registration Fees Details
$ 239 Cost
Registration Ways
Email
Website
Other
Address/Venue
  Online 
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