Seminar - Online
Medical device manufacturers have always been under scrutiny to ensure that their product does no harm to the patient. Regulatory agencies have become increasingly aware of the potential dangers of residual manufacturing materials on medical devices. Therefore, cleanliness has become a hot topic in the medical device community. A thorough validation of the cleaning processes used to remove residual materials from newly manufactured medical devices is necessary to ensure patient safety. One of the most common methods is using extraction techniques to validate the cleanliness of a device. This 60 minutes webinar will provide in-depth and valuable guidance on how to achieve a thorough validation of a cleaning process. Areas Covered in the Session: Cleaning Validation Overview Defining the ScopeIdentifying the Contaminants Choosing the Test Method Choosing the Solvents Setting Extraction Parameters Validating the Extraction Setting LimitsWho Will Benefit:QA/QC managers and personnel Validation managers and personnel Manufacturers of Implantable Medical Devices Manufacturers of Single-Use Medical Devices Manufacturers of Reprocessed/Reusable
Organization: Compliance Trainings (https://compliancetrainings.com )
For more information, please visit: http://bit.ly/1ySG1Wt
Monday, 9 March, 2015 (13:00 - 14:00)
5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada
Online
Phone: 4169154458
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