Test Method Validation to Verify the Performance of a Medical Device

5 years ago Posted By : User Ref No: WURUR29590 0
  • Image
  • TypeWebinar
  • Image
  • Location Fremont, California, United States
  • Price
  • Date 04-04-2019
Webinar Title
Test Method Validation to Verify the Performance of a Medical Device
Event Type
Webinar
Webinar Date
04-04-2019
Last Date for Applying
02-04-2019
Location
Fremont, California, United States
Organization Name / Organize By
Netzealous LLC DBA - Compliance4All
Organizing/Related Departments
Compliance Trainings & Seminars for all Industries
Organization Type
Organization/Company
WebinarCategory
Both (Technical & Non Technical)
WebinarLevel
All (State/Province/Region, National & International)
Related Industries

Education/Teaching/Training/Development

Accounting/Financial/Banking/Insurance

Medical/Healthcare/Hospital

Location
Fremont, California, United States

Overview:
Those who work with process optimization and validation focus on optimizing a process and reducing variability. Those working on Test Method Validation, on the other hand, focus on discerning between process variation and measurement error from the test method itself.

Why should you Attend:
This webinar will help you better understand Test Method Validations to verify the performance of a Medical Device, global reference standards, the FDA requirements and how to perform successful TMV to ensure your inspection of verification is effective, using detailed real-life case studies.

Areas Covered in the Session:
When should Methods be Validated?
Qualification vs Validation
Types of Test Method Validations
How to perform successful test method validations

Who Will Benefit:
Manufacturing Engineers
Regulatory Affairs Teams
Quality Assurance & Quality Control Teams
Operations Teams
Document Control

Speaker Profile:
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. Prior to working full time as a consulting partner for Atzari Consulting, Jose served as Director of Manufacturing Engineering at Boston Scientific and as Quality Systems Manager at Stryker Orthopedics, where he introduced process performance, problem solving, and quality system methodologies.

Event Fee: One Dial-in One Attendee Price: US $150.00

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: [email protected]

Registration Fees
Available
Registration Fees Details
One Dial-in One Attendee Price: $150.00
Registration Ways
Email
Phone
Website
Address/Venue
  Online  Pin/Zip Code : 94539
Official Email ID
Contact
Event Manager

Online

[email protected]

     +1-800-447-9407
   Fax No: 302-288-6884