CFR section

21 CFR 58.33(a): Study director

PART 58-GOOD LABORATORY PRACTICE FOR NONCLINICAL LABORATORY STUDIES · Subpart B-Organization and Personnel

Key facts

Citation 21 CFR 58.33(a)
Section Study director
Part PART 58-GOOD LABORATORY PRACTICE FOR NONCLINICAL LABORATORY STUDIES
Subpart Subpart B-Organization and Personnel
Subchapter 21 CFR A General
Product types cited General
Regulation text (excerpt) (a) The protocol, including any change, is approved as provided by § 58.120 and is followed.

At a glance

  • 10–99 Inspections citing this section
  • 1–9 Warning letters citing this section

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About CFR sections cited by the FDA

Title 21 of the Code of Federal Regulations contains the FDA's regulations, including current good manufacturing practice and quality system requirements that inspections cite.

Source: U.S. Code of Federal Regulations (eCFR); citation statistics from FDA inspection and warning-letter data

Browse all CFR sections cited by the FDA