Vendor Qualification Auditing for FDA Computer System Compliance| Jan. 18, 2012 | Poser

Vendor Qualification Auditing for FDA Computer System Compliance| Jan. 18, 2012 | Poser

July 27th, 2011 // 1:02 pm @

Note: FOI Services ran this event this summer at $449, $100 more than our price. Theirs also was a regular audioconference. This is a Webinar!

This webinar by Dr. Richard Poser, First Quality, Inc., will explain and illustrate inspection and auditing of vendors who provide software used to support GXP manufacturing and testing, through audit forms, processes and checklists. We will explore how vendor qualification audits may be used in the vendor selection process. Case studies and redacted audit reports will be used throughout the presentation.

Note: All Webinars are eligible for 1.0 CEU towards RACS Certification and 0.1 RU towards ASQ Certification.

Feedback from this event: “Dr. Poser, thank you for the wonderful training webinar this afternoon. I would greatly appreciate the documentation/templates that you described.”

“Greetings Dr. Poser, you put on an excellent presentation this afternoon with excellent suggestions and tools that can be applied. I am requesting the sample of documents you used today. Thank you.”

We will show how audit findings of competitive vendors may be used to select products and negotiate pricing and terms. We will examine the audit process from initial request to conduct an audit through the conduct of on site inspection, closing meetings and audit reports.

Illustrations of observations and remediation plans will be used throughout. The various types of audits will be discussed, including initial qualification, remediation, routine, for cause and correspondence. The seminar will include sample forms and checklists which may be used by the participants, along with some initial training on the appropriate use of forms and checklists.

Group Price: $349 ($50 Off Regular Price)

Add to Cart

Recording Only (Download or CD): $299
Add to Cart

Areas Covered in the seminar:

  • Audit types.
  • Pre-audit materials.
  • Conducting site inspections.
  • Closing meetings.
  • Writing audit observations, recommendations and remediation.
  • Use of audits in vendor qualification and selection.

Who will benefit:
This webinar will provide valuable assistance to all regulated companies that need to prepare for inspection of the facilities, including companies in the Medical Device, Diagnostic, Pharmaceutical, and Biologics fields. Contract facilities providing clinical, laboratory and data systems will also benefit.

The employees who will benefit include:

  • End-users responsible for testing
  • QA managers and validation personnel
  • Information systems managers and personnel
  • Senior Quality, Facilities and R&D Management
  • Regulatory Affairs staff
  • Quality system auditors

Attendees will receive these free gifts:

  • Subscription to FDA Digest – 483/warning letter e-newsletter
  • Six-month subscription to SMARTERCOMPLIANCEâ„¢ newsletter by Cerulean Associates ($129 value)
  • Expert, easy-to-grasp guide on Quality-by-Design, (QBD) by Cerulean Associates
  • “Lean Compliance for Midsized Companies” (from Journal of GXP Compliance, January 2008)

About The Presenter:

Rich Poser, is President of First Quality Inc., a quality consulting firm focused on Quality Systems, Training and Validation. Their clients include biotechnology, pharmaceutical and medical device manufacturers, as well as the vendors such as contract laboratories, instrument manufacturers, contract manufacturing sites and software developers that support these highly regulated industries.

Dr. Poser was Director of Analytical Sciences and later Director of Information Systems at the Fisons Pharmaceuticals site in Rochester, NY. Following work in product development, laboratory automation, and validation and quality systems for the Mylan Pharmaceutical Company, Rich joined Dura Pharmaceuticals in San Diego as Analytical Laboratory Director and Director of R&D Quality Assurance. After the acquisition of Dura by Élan, Rich was appointed Director of Quality Laboratory Operations and led their 21CFR Part 11 training and audit team.

Now in private practice as a quality consultant, he also lectures at UCSD Extension in validation, cGMP Regulations and analytical methods validation, and has presented or chaired public seminars and symposia.

Group Price: $349 ($50 Off Regular Price)

Add to Cart

Recording Only (Download or CD): $299
Add to Cart

Subscribe Now

Featured Partner