Design Validation Procedures

Design validation procedures refer to a set of activities performed to ensure that your design is capable of meeting user defined specifications and requirements. ADB Consulting’s state of the art design validation procedures for medical devices help the manufacturers have a clear view into their product design and possible errors.

We provide a package of design validation services that will meet all your regulatory requirements for ISO and FDA approval. ADB provides assurance to medical device industries that the design process has been planned, is progressing according to plan and meets the needs of your stakeholders.

Our industry-leading experts follow a comprehensive and systematic examination process to evaluate the adequacy of the design requirements. The entire process is then followed by a risk management assessment and a detailed documentation to provide evidence that your medical device consistently meets specified requirements. Our time-tested validation processes detect and address problems effectively and inexpensively so as to avoid costly rework later during post-deployment phases.


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