21 CFR 822.11 - What should I consider when designing my plan to conduct postmarket surveillance?

Code of Federal Regulations - Title 21: Food and Drugs

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Title 21: Food and Drugs

CHAPTER I: FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED)

SUBCHAPTER H: MEDICAL DEVICES

PART 822: POSTMARKET SURVEILLANCE

Subpart C: Postmarket Surveillance Plan

822.11 - What should I consider when designing my plan to conduct postmarket surveillance

You must design your surveillance to address the postmarket surveillance question identified in the order you received. You should consider what, if any, patient protection measures should be incorporated into your plan. You should also consider the function, operating characteristics, and intended use of your device when designing a surveillance approach.

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