Auditing Strategies for Cleaning Processes and Cleaning Validation

Instructor: John Hyde
Product ID: 701185
  • 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: Mar-2009

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 Pharmaceutical compliance training will provide valuable assistance to all regulated companies that need to validate and audit their equipment cleaning processes.

Cleaning is an essential unit operation in the manufacture of biopharmaceutical products. As biopharmaceutical process technologies have improved and matured, cleaning methodologies and strategies and practices of cleaning validation have followed suit to provide higher levels of assurance of effective, repeatable and reliable operation.

This session will address auditing strategies for cleaning processes and cleaning validation for pharmaceutical and biopharmaceutical process systems and equipment.

Areas Covered in the seminar:

  • Chemical and physical bases for current practices of cleaning processes and cleaning validation.
  • Recent FDA comments and observations with respect to cleaning validation and ongoing monitoring.
  • Auditing strategies for effective management of OOS events and excursions.
  • Risk-based approaches to cleaning validation and ongoing monitoring of cleaning operations.

Who will benefit:

This webinar will provide valuable assistance to all regulated companies that need to validate and audit their equipment cleaning processes, including companies in the Biopharmaceutical, Pharmaceutical and Medical Device fields. The employees who will benefit include:

  • Quality Assurance professionals and mangers
  • Validation professionals, practitioners and mangers
  • Operations professionals and mangers
  • Engineering professionals and managers
  • Regulatory professionals

Instructor Profile:

John Hyde, is the Founder and Chairman of the Board for Hyde Engineering + Consulting, a firm of 80 professionals specializing in providing process systems design, commissioning, validation and FDA compliance services to biopharmaceutical and pharmaceutical manufacturers.

John has presented papers at numerous engineering conferences and short courses on topics including biopharmaceutical process systems design, cleaning and cleaning validation principles and practices, FDA compliance strategies, and control systems design for manufacturing processes. He has published ten articles on these subjects.

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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.

We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email call +1-888-717-2436 (Toll Free).

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