The purpose of this Procedure is to define what validation is, which processes need to be validated, and which records are necessary in order for all processes necessary for the manufacturing of the medical device to be kept under continuous control. This procedure does not cover the software validation, which is included in the Procedure for Documentation and Validation of Computer Software.
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There is 1 appendix related to this document. The appendix is not included in the price of this document and can be purchased separately: Validation Master Plan.
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