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