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

Training CD

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

Customer Care

Fax: +1-650-963-2556


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.

Follow us :
ComplianceOnline Banking Summit 2016 | Risk Management and Data Security - 80390SEM
21 CFR Part 11 Compliance for SaaS/Cloud Applications - 80202SEM

Product Reviews

This product hasn't received any reviews yet. Be the first to review this product! Write review

Best Sellers
You Recently Viewed