Cleaning Validations Using Extraction Techniques
Website https://www.onlinecompliancepanel.com/webinar/Cleaning-Validations-Using-Extraction-Techniques-50779 |
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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 PresentationImportance of device cleanliness and cleanabilityBasics of validating a cleaning processChoosing test soils based on target contaminantsAvailable test methods for cleaning validationsValidation of the extraction methodEstablishing and justifying residue limitsFor Registration:https://www.onlinecompliancepanel.com/webinar/Cleaning-Validations-Using-Extraction-Techniques-507793/DECEMBER-2017-ES-OURGLOCAL
Website: https://www.onlinecompliancepanel.com/homeNote: 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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