Log in or Subscribe Now to 483sOnline.com to get critical documents on what medical device companies should do before, during and after an FDA inspection. You can find everything from how to prepare your facility for an inspection, to managing the inspection, to tips on how to work with regulators to solve deficiencies.
Here you will find resources that will keep your firm in constant readiness for the investigator’s next visit. You’ll find expert advice, compliance guidance and best practices that you can put into practice today. Click here to find out more.
The investigators are in the building. What procedures will they follow? How do you handle record and photography requests, manage the war room, or challenge a false observation? Click here to find out more.
After the inspectors leave, you still have plenty to do. For information about post-inspection deadlines, best practices for responding to 483s, and details on the enforcement options that you may face. Click here to find out more.
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