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1. www.accessdata.fda.gov › CFRsearchCFR - Code of Federal Regulations Title 21 - Food and Drug ...

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   Dec 22, 2023 · Subpart B - Informed Consent of Human Subjects § 50.20 - General requirements for informed consent. § 50.22 -

   • Subpart a - General Provisions

     (b) References in this part to regulatory sections of the...

   • 21 CFR 50, Subpart B

     PROTECTION OF HUMAN SUBJECTS. Subpart B - Informed Consent...

2. ecfr.io › Title-21 › Part-50Title 21 Part 50 Subpart B - Code of Federal Regulations

   ecfr.io › Title-21 › Part-50

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   Subpart B - Informed Consent of Human Subjects. Source: 46 FR 8951, Jan. 27, 1981, unless otherwise noted.

3. www.law.cornell.edu › cfr › text21 CFR Part 50 - PART 50—PROTECTION OF HUMAN SUBJECTS

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   Electronic Code of Federal Regulations (e-CFR) Title 21—Food and Drugs. CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES. SUBCHAPTER A—GENERAL. PART 50—PROTECTION OF HUMAN SUBJECTS.

4. www.law.cornell.edu › cfr › text21 CFR Subpart B - Subpart B—Informed Consent of Human ...

   www.law.cornell.edu › cfr › text

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   Electronic Code of Federal Regulations (e-CFR) Title 21—Food and Drugs. CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES. SUBCHAPTER A—GENERAL. PART 50—PROTECTION OF HUMAN SUBJECTS. Subpart B—Informed Consent of Human Subjects.

5. www.ecfr.gov › subchapter-A › part-50eCFR :: Home

   www.ecfr.gov › subchapter-A › part-50

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6. ecfr.io › Title-21 › Part-5021 CFR §50 Protection Of Human Subjects - Code of Federal ...

   ecfr.io › Title-21 › Part-50

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   Title 21, part 50 of the Electronic Code of Federal Regulations.