The 21 CFR Part 314 Subpart H meaning is Subpart of Part 314 pertaining to accelerated approval of drugs. patent. Subpart B_Applications. The Medical Acronym / Slang 21 CFR Part 314 Subpart H means... AcronymsAndSlang. There are 3 types of searches that can be done on the CFR Title 21 database. Amendment: A proposal to alter the text of a pending bill or other measure by striking out some of it, by inserting new language, or both.Before an amendment becomes part of the measure, thelegislature must agree to it. 201, 501, 502, 505, 506, 507, 512, 701, 704 of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. Hop on to get the meaning of 21 CFR Part 314 Subpart H acronym / slang / Abbreviation.

21 Code Federal Regulations Part 316 - Orphan Drugs Public Law 97-414 To amend Federal Food, Drug, and Cosmetic Act to facilitate the development of drugs for rare diseases and conditions in PDF The Definition of 21 CFR Part 314 Subpart H is given above so check it out related information.

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Provides the text of the 21 CFR 314.150 - Withdrawal of approval of an application or abbreviated application.

The Medical Acronym / Slang 21 CFR Part 314 Subpart H means... AcronymsAndSlang. Subpart A - General Provisions (§§ 314.1 - 314.3) Subpart B - Applications (§§ 314.50 - 314.90) Subpart C - Abbreviated Applications (§§ 314.92 - 314.99) APPLICATIONS FOR FDA APPROVAL TO MARKET A NEW DRUG; Subpart B. Subpart A_General Provisions.

314.1 Scope of this part. CFR ; prev | next. Evidence: Information presented in testimony or in documents that is used to persuade the fact finder (judge or jury) to decide the case for one side or the other. Applications; Section 314.70. 21 CFR Part 314 Subpart H definition / 21 CFR Part 314 Subpart H means? The meaning of the 21 CFR Part 314 Subpart H is also explained earlier. 314.3 Definitions. Electronic Code of Federal Regulations (e-CFR) Title 21. § 314.162 - Removal of a drug product from the list. 314.550 Promotional materials. Hop on to get the meaning of 21 CFR Part 314 Subpart H acronym / slang / Abbreviation. 314.52 Notice of certification of invalidity or noninfringement of a .

Terms Used In 21 CFR 314.3.

I verify under penalty of perjury that the foregoing is true and correct. § 314.170 - Adulteration and misbranding of an approved drug. 21 CFR Part 314 - APPLICATIONS FOR FDA APPROVAL TO MARKET A NEW DRUG . The 21 CFR Part 314 Subpart H meaning is Subpart of Part 314 pertaining to accelerated approval of drugs.

§ 314.160 - Approval of an application or abbreviated application for which approval was previously refused, suspended, or withdrawn. It is divided into three chapters: Chapter I — Food and Drug Administration Chapter II — Drug Enforcement Administration Part 314 - Applications For Fda Approval To Market A New Drug. '; Toggle navigation eCFR. Supplements and other changes to an approved NDA. CFR › Title 21 › Volume 5 › Chapter I › Subchapter D › Part 314. FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES; Subchapter D. DRUGS FOR HUMAN USE; Part 314. (21 CFR Part 211 As of April, 1996) Authority: Secs. 38 Appendix J Form FDA 1639 (and Instructions) • • 4 2 . 21 CFR 314.80 . § 314.550 Promotional materials. I attest that I am familiar with 21 CFR 314.53 and this submission complies with the requirements of the regulation. Food and Drugs; Chapter I.

Governmental » FDA.

Home; Title 21 PART 314. There are 3 types of searches that can be done on the CFR Title 21 database. Title 21 is the portion of the Code of Federal Regulations that governs food and drugs within the United States for the Food and Drug Administration (FDA), the Drug Enforcement Administration (DEA), and the Office of National Drug Control Policy (ONDCP).. 314.53 Submission of patent information. 314.50 Content and format of an application. The 21 CFR Part 314 Subpart H acronym/abbreviation definition. This time-sensitive patent information is submitted pursuant to 21 CFR 314.53. Terms Used In 21 CFR 314.200. 21-CFR-314: APPLICATIONS FOR FDA APPROVAL TO. (CFR). What is the meaning of 21 CFR Part 314 Subpart H? 314.2 Purpose. I.

§ 314.161 - Determination of reasons for voluntary withdrawal of a listed drug. That subpart of 21 CFR Part 314 pertaining to accelerated approval of drugs. The 21 CFR Part 314 Subpart H acronym/abbreviation definition.

Title 21, part 314 of the Electronic Code of Federal Regulations. MARKET A NEW DRUG--Table of Contents.