Why waste your valuable time writing SOP's. Better to spend your time solving your client's problems. You can produce higher quality documents quickly. SOP's include forms that are time consuming to create.
Why risk a 483 by accidentally omitting information in your custom SOP.
Our SOP's are up to the minute in meeting FDA expectations. They are based on extensive industry experience and have passed FDA audits. They are continually updated based on feedback from users and new FDA requirements. They are easily customizable to fit your clients specific situation.
Use Medical Device SOP Advisors as your reference library of device SOP's.
Our guarantee is to rewrite at no charge any SOP that results in a 483 or other agency observation..
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