You have a Sterility Failure or Bioburden Excursion - Now What?
Compliance training on Sterility or Bioburden test failures, items to be investigated to determine the root cause and the follow up to the investigation.
Reducing Ethylene Oxide (EO) Sterilization Costs While Maintaining Regulatory...
Instructor: Marisel Ortiz In this Ethylene Oxide (EO) Sterilization training, you will learn how to evaluate your sterilization process for cost reduction/process efficiency, and also...
2-day In-person Seminar: Medical Device Sterilization: Corrective & Preventiv...
The course will begin with an overview of EO sterilization, explaining which aspects of the process often cause confusion
Hotel chain rolls out UV sterilization
Out of sight, out of mind. That's a mantra hotel guests tend to adopt as they tuck into rooms inhabited by hundreds of previous guests -- and possibly the microscopic germs and debris...
You have a Sterility Failure or Bioburden Excursion
This Sterility or Bioburden test Webinar/training will discuss on various items that should be investigated to determine the root cause and the follow up to the investigation. Why Should...
Application of CAPA to the Device Sterilization Process
Do you use a Contract Sterilizer for your medical device sterilization? Are you not an expert in industrial sterilization? If you answered “yes” to either of these questions, this seminar...
Submission Documentation for Sterilization Process Validation - A Comprehensi...
Instructor: Colin Davis In this sterility assurance documentation webinar, you will learn specifically what information is required in sterility assurance documentation for injectable...
Submission Documentation for Sterilization Process Validation
In this sterility assurance documentation webinar, you will learn specifically what information is required in sterility assurance documentation for injectable drug products and how to...
Application of CAPA in (Device) Sterilization – For the Non-Expert
This webinar will review the typical non-conformances experienced in the (Medical Device) sterilization process and the course of action that should be taken by the manufacturer or...
Testing considerations for sterilization validation and routine sterilization...
Instructor: Gerry O Dell This sterilization validation process training webinar will review the FDA or ISO requirements for tests following validation and emphasis is placed on the...