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Cleaning Validations Using Extraction Techniques

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Category medical device cleaning validation, cleaning and disinfecting medical equipment, cleaning disinfection and sterilization of medical equipment, medical cleaning solutions , cleaning medical devices, cleaning medical instruments, FDA Reprocessing Guidance, Extraction validations, Extraction Techniques, test methods for cleaning validations, test soil, residue limits, Setting extraction parameters, Validating the extraction, patient safety, patient safety in hospitals, patient safety goals, cleaning validation in pharma , test your soil , cleaning validation in pharmaceutical industry

Deadline: December 04, 2017 | Date: December 05, 2017

Venue/Country: Online, U.S.A

Updated: 2017-11-14 21:23:21 (GMT+9)

Call For Papers - CFP

Cleaning validations are an essential step in the medical device development process. One of the most common methods is using extraction techniques to validate the cleanliness of a device. This webinar will provide valuable guidance on how to achieve a thorough validation of a cleaning process. These cleaning processes may include initial cleaning validations, in process cleaning validations, or reprocess cleaning validations.

Objectives of the Presentation

Importance of device cleanliness and cleanability

Basics of validating a cleaning process

Choosing test soils based on target contaminants

Available test methods for cleaning validations

Validation of the extraction method

Establishing and justifying residue limits

For Registration:


Note: Use Promo Code HYED6Z and get 10% off on registration (Valid till DECEMBER 31st 2017)

Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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