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Microbiological Issues in Cleaning Validation and How to Control Bioburden

: 25 Apr 2019

Sector: Pharmaceutical

Type: Webinar


This Live Webinar takes place at 10.30 AM -12.30 PM ET (New York Time)

 

Control of microorganisms by effective cleaning processes is important for both non-sterile and sterile manufacturing processes. This interactive live training will focus on the issues involved with bioburden and other related microbiological topics for cleaning validation. It will start with a discussion of why we address microbiological issues in cleaning validation, as well as ways to control bioburden. It will then cover setting limits, sampling, and sampling recovery studies. A major focus of microbiological issues for many regulatory guidelines is prevention of bioburden proliferation following cleaning and before use. Various clean hold time issues, such as ways to minimize proliferation and to set acceptance criteria, will be addressed. Bioburden in cleaning validation is also one of the main ways that companies can leverage data from other studies based on the new FDA process validation guideline. Finally, related biological concerns, such as endotoxin, will be discussed.

 

Learning Benefits:

  • Understanding the terminology applied to bioburden for cleaning validation.
  • Learn control measures for bioburden during the cleaning process.
  • Understanding and applying swab and rinse limits for bioburden, including carryover calculations and industry standard practices.
  • Understanding limits determination for endotoxins based on industry standard practices.
  • Understanding and applying sampling and sampling recovery studies.
  • Evaluating bioburden during clean hold time studies.
  • Learn what regulatory documents say about microbiological control.

 

This live training webinar includes the following for each registered attendee:

  • A copy of the presentation slides
  • A certificate of training for attendee records

 

This live training webinar is applicable to drug product manufacturers and API manufacturers, including biopharmaceutical manufacturers.

 

The following individuals or disciplines involved in process equipment cleaning validation will benefit from attending this live webinar:

  • Microbiology personnel
  • Senior management responsible for cleaning validation Validation, Quality Control, Quality Assurance, Manufacturing, Regulatory Affairs, Technical Support
  • Directors, Managers/Supervisors, Scientists, Technicians, Operators, Auditors
  • Regulatory Affairs Professionals

Find out more / register here:

Venue


Organizer

PHARMA WEBINARS
Phone: +1 (877) 792.7587
Email: support@pharmawebinars.com
Visit: http://www.pharmawebinars.com


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IAFPs European Sympo...
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Regulatory Aspects o...