Standard Guide for Validating Cleaning Processes Used During the Manufacture of Medical Devices
|Publication Date:||1 April 2016|
This guide provides considerations for validating cleaning processes for medical devices during initial fabrication and assembly prior to initial use. Validated cleaning processes are important for achieving consistency in function and consistency in biocompatibility. The considerations include but are not limited to, validation approach, equipment design, procedures and documentation, analytical methods, sampling, development of limits, and other issues.
This guide describes the validation of critical cleaning processes for medical devices to reduce contaminants to acceptable levels prior to packaging.
Reusable medical devices.
Validation of cleaning operations for reusable medical devices is not within the scope of this standard guide. Although cleaning of reusable medical devices is beyond the scope of this guide, many of the principles outlined in this guide may be applicable to the validation of cleaning operations for reusable devices.
Cleaning of medical devices in health care facilities.
Validation of cleaning processes in patient/health care facilities is not within the scope of this standard guide.
This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.