Cleaning Validation Made Easy : Basic Concepts of Cleaning Validation

Instructor: Victor Olatundun
Product ID: 706346
  • Duration: 60 Min
This webinar will discuss the basic concepts associated with cleaning validation to facilitate the construction of robust cleaning validation program as well as provide a cost-effective approach on conducting cleaning validation.
Purchase option for this webinar is currently unavailable. Please contact our Customer Care for more info.

Customer Care

Fax: +1-650-362-2367

Email: customercare@complianceonline.com

Read Frequently Asked Questions

Why Should You Attend:

Regulatory body citations (FDA warning letters, 483 Observations etc) on the subject on cleaning validation has been a never-ending story of audit findings due to the lack of understanding of basic concepts of cleaning validation or nonchalant attitude towards this aspect of validation. Without a robust cleaning validation program, manufacturing operations and/or schedules can be negatively impacted if major cross contamination issues are prevalence in the routine manufacturing processes. The continuous disruption of manufacturing operations could subsequently lead to loss in revenue due to fines associated late product delivery to market and/or clients as well as inability to make and sell products due to halted manufacturing operations associated with such major citations. Therefore, gaining knowledge and understanding in the basic concepts of cleaning validation and knowing how to apply them, could be a major turning point for a firm that has been plagued with ongoing citations association with cleaning validation.

Cleaning validation has been misconstrued over the years basically due to lack of understanding of the cleaning validation concepts. Cleaning validation is predominantly associated with processing equipment involved in drug manufacture and not the room or environment in which the product is made, consequently delineating cleaning validation from environmental monitoring. Additionally, the cleaning validation program can be designed in a cost-effective way with better understanding of the concepts like DEHT, CEHT, TACT( cleaning steps) as well as a clear understanding of product and cleaning agent chemistry.

Attending this webinar will highlight on the “what”, “why”, “when”, “who” and “how” elements of cleaning validation to facilitate the better cleaning validation program design for success. Attendees will gain a better understanding of cleaning validation concepts and know how these concepts fit into the design of robust and effective cleaning validation program to satisfy both company’s quality compliance objectives and regulatory body standards.

Areas Covered in the Webinar:

  • Cycle Development
  • Cleaning SOP
  • Dirty Equipment Hold Time (DEHT)
  • Clean Equipment Hold Time(CEHT)
  • Campaign Length
  • Periodic Monitoring Program
  • Sampling Techniques (Swab & Rinse Samples)
  • Continued Process Verification
  • Critical Process Parameters
  • TACT ( Time, Action, Concentration, Temperature)
  • Analytical Test Method

Who Will Benefit:

  • R&D Scientists and/or Technicians
  • Process Development Scientists / Technicians
  • Technology Transfer Technologist
  • Validation Personnel
  • Manufacturing Operation Group Leader/ Supervisors
  • Quality Assurance Team Leads

From the following industries:

  • Biologics, Pharmaceuticals, Vaccines, Medical Devices etc.

Free Materials:

  • FDA 2011 Process Validation Guideline
  • Technical Report # 29: Points to Consider for Cleaning Validation
  • Technical Report# 49: Points to Consider for Biotechnology Cleaning Validation
Instructor Profile:
Victor Olatundun

Victor Olatundun
Management Consultant, Validant

Victor Olatundun is a pharmaceutical professional with 25 years expertise in the field of validation, technology transfer, management consulting and quality system remediation strategy in the biologics and pharmaceutical industry. He possesses strong leadership and management skills coupled with strong technical expertise, process knowledge and understanding in the field of validation and manufacturing operations. Additionally, he possesses both hands-on expertise and a strategic view of all aspects of the validation relating to process, cleaning, shipping and commissioning & qualification projects.

Follow us :
Reduce costs for compliance with data integrity: 21 CFR Part 11, SaaS/Cloud, EU GDPR

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 customercare@complianceonline.com call +1-888-717-2436 (Toll Free).

Product Reviews

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

Best Sellers
You Recently Viewed
    Loading