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Qualification of Equipment as Part of Process Validation for Medical Devices

An essential part of quality management according to the General Medicine Act (MPG) and the US Food and Drug Administration's (FDA) Code of Federal Regulations (CFR), is the validation of all processes, and equipment/computer-controlled systems which have a direct impact on the quality of product manufacturing. Process validation is defined as the collection and evaluation of data from the process design stage throughout production, which establishes scientific evidence that a process is capable of consistently delivering quality products.  

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DOWNLOAD WHITEPAPER

Qualification of Equipment as Part of Process Validation for Medical Devices

An essential part of quality management according to the General Medicine Act (MPG) and the US Food and Drug Administration's (FDA) Code of Federal Regulations (CFR), is the validation of all processes, and equipment/computer-controlled systems which have a direct impact on the quality of product manufacturing. Process validation is defined as the collection and evaluation of data from the process design stage throughout production, which establishes scientific evidence that a process is capable of consistently delivering quality products.  

Download to find out more.

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