What is a CFR test?

What does CFR stand for in law?

The Code of Federal Regulations
The Code of Federal Regulations (CFR) is the codification of the general and permanent rules published in the Federal Register by the executive departments and agencies of the Federal Government.

What is a CFR test?

Coronary Flow Reserve (CFR) quantification, used in conjunction with Myocardial Perfusion Imaging (MPI), can potentially help to rule out Coronary Artery Disease (CAD). Coronary Flow Reserve compares the myocardial blood flow at peak hyperemia (stress) with the myocardial blood flow at rest.

What is Subpart H approval?

Subpart H – Accelerated Approval of New Drugs for Serious or Life-Threatening Illnesses.

What does CFR stand for in OSHA?

the Code of Federal Regulations
What is OSHA 29 CFR 1910? For reference and enforcement, the rules created by all federal regulatory agencies are collected into a multi-part document called the Code of Federal Regulations (CFR). Within the CFR, regulations are organized by the governing department and the topic of the rules.

Is CFR legally binding?

The first edition of the CFR was published in 1938, and it has since gone through many changes. These rules are considered legally binding just as any statute. The Office of the Federal Register publishes the CFR annually in 50 titles.

What is this thing as per US Coastguard CFR 33 that ur required to do atleast 12hrs prior arrival port?

33 Code of Federal Regulations 164.25 (please see below)states no person may cause a vessel to enter into or get underway on the navigable waters of the United States unless no more than 12 hours before entering or getting underway, the main steering gear is tested from the alternative power supply (emergency generator …

What is Subpart E FDA?

LICENSING. Subpart E – Accelerated Approval of Biological Products for Serious or Life-Threatening Illnesses.

What does CFR stand for in manufacturing?

Cost and Freight (CFR) Definition.

What are the 314 § of the FDA?

§ 314.102 – Communications between FDA and applicants. § 314.103 – Dispute resolution. § 314.104 – Drugs with potential for abuse. § 314.105 – Approval of an NDA and an ANDA. § 314.106 – Foreign data.

What is the Code of Federal Regulations (CFR)?

The Code of Federal Regulations (CFR) is the official legal print publication containing the codification of the general and permanent rules published in the Federal Register by the departments and agencies of the Federal Government. The Electronic Code of Federal Regulations (eCFR) is a continuously updated online version of the CFR.

Is there a preview of Article 314 in NFPA 70?

Below is a preview of Article 314. See the actual NEC text at NFPA.ORG for the complete code section. Once there, click on their link to free access to the 2017 NEC edition of NFPA 70. 314.20 In Wall or Ceiling.

What are the nomenclature changes to Part 314?

Nomenclature changes to part 314 appear at 69 FR 13717, Mar. 24, 2004; 81 FR 69639, Oct. 6, 2016. § 314.80 Postmarketing reporting of adverse drug experiences. ( a) Definitions. The following definitions of terms apply to this section: Adverse drug experience.