Max Sherman, editor
The Medical Device Validation Handbook is a unique and essential compilation of the regulatory professional’s role in the validation and verification processes of medical devices. Since international validation standards change with new iterations, this handbook helps you remain current on validation guidelines and quality control measures needed to comply with federal and international requirements. Each chapter is written by an expert in the field.
The handbook is essential for medical device companies who depend on their employees’ understanding of validation and verification processes. This includes regulatory, design and development, management, quality, packaging engineers, sterilization, software and manufacturing engineers. The information provided can be applied as easily to small companies as to larger firms.
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