Process Validation for Medical Devices - The Regulatory Approach

Instructor: Dan OLeary 
Product ID: 702673
Training Level: Intermediate to Advanced
  • Duration: 90 Min

recorded version

1x Person - Unlimited viewing for 6 Months
(For multiple locations contact Customer Care)
Recorded Link and Ref. material will be available in My CO Section
Last Recorded Date: Jan-2013

Training CD / USB Drive

One CD/USB is for usage in one location only.
(For multiple locations contact Customer Care)
CD/USB and Ref. material will be shipped within 15 business days

Customer Care

Fax: +1-650-362-2367


Read Frequently Asked Questions

This medical device process validation training will use recent warning letters to explain the regulatory requirements for process validation and what FDA Investigators look for. It will cover process validation components (IQ, OQ, and PQ), and the content of protocols and reports.

Why Should You Attend:

Process validation is one of the most common citations in medical device Warning Letters. This webinar explains the fundamental requirements for process validation with a focus on FDA QSR, but includes ISO 13485:2003. You will learn the regulatory requirements for process validation, the traditional components of process validation (IQ, OQ, and PQ), and the content of protocols and reports. The webinar examines FDA Warning Letters to help understand the requirements and explain what FDA Investigators look for. Because FDA Investigators follow the Quality System Inspection Technique (QSIT), the webinar explains the objectives and links them to the regulation and the Warning Letters.

Areas covered in this webinar:

  • The process validation requirements in FDA QSR.
  • The process validation requirements in ISO 13485:2003.
  • Applying the traditional approach to IQ, OQ, & PQ.
  • The QSIT approach and how FDA Investigators apply it.
  • Warning Letters and how to learn from them.

Who Will Benefit:

The following personnel from medical device companies will benefit

  • Design Engineers, especially engineers responsible for design transfer
  • Manufacturing Engineers
  • Quality Engineers
  • Quality Auditors
  • Regulatory Affairs
  • Quality Systems Personnel
  • R&D and Engineering Staff
  • Risk Managers
  • Production Supervisors

Instructor Profile:

Dan , is the President of Ombu Enterprises, LLC, a company offering training and execution in Operational Excellence, focused on analytic skills and a systems approach to operations management. Dan has more than 30 years experience in quality, operations, and program management in regulated industries including aviation, defense, medical devices, and clinical labs. He has a Masters Degree in Mathematics; is an ASQ certified Biomedical Auditor, Quality Auditor, Quality Engineer, Reliability Engineer, and Six Sigma Black Belt; and is certified by APICS in Resource Management.

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Refund Policy

Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.

Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.

If you have any concern about the content of the webinar and not satisfied please contact us at below email or by call mentioning your feedback for resolution of the matter.

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