Good Guidance Practice (GGP) documents are documents prepared for CDRH staff, regulated industry and the public that relate to:
Guidance documents do not create or confer any rights for or on any person and do not operate to bind FDA or the public. An alternative approach may be used if such approach satisfies the requirements of the applicable statue, regulations, or both.
Most guidance documents exist on the Web and are available via the GGP search engine.
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Office of Compliance |
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OCD
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Office of the Center Director |
ODE
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Office of Device Evaluation |
OCER
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Office of Communication, Education, and Radiation Programs |
OMO |
Office of Management Operations |
OSB
|
Office of Surveillance and Biometrics |
OSEL
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Office of Science and Engineering Laboratories |
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Updated June 2, 2006
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