Web( c) It shall be unlawful for any person to abuse any exemption or exception to the requirements of section 2 (h) of the Act, including any exemption or exception as the Commission may provide by rule, regulation, or order. § 50.11-50.24 [Reserved] Subpart B - Clearing Requirement Compliance Schedule and Compliance Dates
eCFR :: 21 CFR 50.20 -- General requirements for informed consent.
WebJan 17, 2024 · A sponsor shall submit a protocol amendment when a new investigator is added to carry out a previously submitted protocol, except that a protocol amendment is not required when a licensed... Web(e) (1) Obtaining informed consent for investigational in vitro diagnostic devices used to identify chemical, biological, radiological, or nuclear agents will be deemed feasible … parking at oxford parkway station
eCFR :: 21 CFR Part 50 -- Protection of Human Subjects
Web( 6) A clinical investigation involving an exception from informed consent under § 50.24 of this chapter is not exempt from the requirements of this part. ( c) Bioavailability studies. The applicability of this part to in vivo bioavailability studies in humans is subject to the provisions of § 320.31. ( d) Unlabeled indication. Web5 CFR § 2424.50 - Illustrative criteria. CFR § 2424.50 Illustrative criteria. A compelling need exists for an agency rule or regulation concerning any condition of employment when the … WebNavigate by entering citations or phrases (eg: 1 CFR 1.1 49 CFR 172.101 Organization and Purpose 1/1.1 Regulation Y FAR). Choosing an item from citations and headings will bring you directly to the content. Choosing an item from full text search results will bring you to those results. Pressing enter in the search box will also bring you to ... timex t235 clock radio manual