21 C.F.R. · Food and Drugs
21 C.F.R. § 822.25

What are my responsibilities after my postmarket surveillance plan has been approved?

Title 21 C.F.R. ● ACTIVE Primary Source
Regulatory Text

21 C.F.R. § 822.25 — What are my responsibilities after my postmarket surveillance plan has been approved?

§ 822.25 What are my responsibilities after my postmarket surveillance plan has been approved? After we have approved your plan, you must conduct the postmarket surveillance of your device in accordance with your approved plan. This means that you must ensure that: (a) Postmarket surveillance is initiated in a timely manner; (b) The surveillance is conducted with due diligence; (c) The data identified in the plan is collected; (d) Any reports required as part of your approved plan are submitted to us in a timely manner; and (e) Any information that we request prior to your submission of a report or in response to our review of a report is provided in a timely manner.

Source: ecfr.gov · govinfo.gov — public domain Official Source ↗
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BS-CFR21-SEC-4608A7
Entity Class
REGULATION / FEDERAL-CFR-SECTION
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boisestandard.org
Citation
21 C.F.R. § 822.25
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CFR — Code of Federal Regulations
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PRIMARY-SOURCE
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✓ TRUE
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930afc9fbabe4c90...
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The regulatory text of 21 C.F.R. § 822.25 is reproduced from the official Code of Federal Regulations as published by the Office of the Federal Register and the National Archives and Records Administration.
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boisestandard.org United States Law CFR Title 21 21 C.F.R. § 822.25