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Basics of Testing Associated with Sterilization Validation and Routine Processing

Date: 01-Mar-12 to 01-Mar-12
Location: Online Webinar / California City / United States
Category: Healthcare & Pharmaceuticals

This sterilization validation process training webinar will review the FDA or ISO requirements for tests following validation and emphasis is placed on the appropriate tests for validation, the appropriate routine tests and the frequency of testing.
All sterilization methods require validation and during this validation they must demonstrate that products meet the required sterility assurance level, that the product remains function and is safe for use. Manufacturers do not always understand the scope of this testing, the applicable standards and how it should be applied to the product they produce with their designated sterilization method. Following validation during routine production some testing is required but often manufacturers are not sure of what testing is required, the frequency necessary and how much flexibility they have in the testing.
Areas Covered in the seminar:

* What are the appropriate types of tests during sterilization validation.
* What standards should be used for the testing.
* What type of samples and sample sizes should be used.
* What testing needs to be performed routinely.
* What frequency of testing is recommended.
* What methods can be used to reduce testing.
* Important testing considerations for validations and routine testing.

Visitors

* QA personnel
* Validation specialists
* Manufacturing personnel involved in validations
* R&D specialists

Exhibitors

At ComplianceOnline, we are focused on :
Enhancing global compliance, creating a world where quality and compliance professionals, regulators,and government agencies come together to help the world comply with the intent and the spirit of laws, policies and mandates, ensuring continuous improvement in global operations, quality & safety.
Making sure that we are responsible corporate citizens helping our constituents build a more responsible enterprise, one which operates with high quality , under a code of ethics, and with process discipline to ensure greater shareholder returns.
Keeping things simple and straight forward , so that we all can indeed improve the quality of our processes, our work, our businesses and enhance compliance globally.
Being inclusive, giving the process experts ( & novices! ), compliance professionals, quality champions, and regulatory agencies a voice so that all of us can contribute and make a difference.

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