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FDA Abbreviations


Browse all acronyms and abbreviations related to the FDA terminology and jargon.

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4158 Abbreviations & Definitions of Acronyms FDA in category Governmental

Browse All Abbreviation related to the Acronym FDA. All abbreviations on this page are (b)(4) means Freedom of Information Act Exemption 4, which protects from disclosure ôtrade secrets and commercial, 1932 means FDA form for veterinary adverse drug reaction, lack of effectiveness, product defect report--mandatory, 1932a means FDA form for veterinary adverse drug reaction, lack of effectiveness, product defect report--voluntary, 21 CFR Part 314 Subpart H means Subpart of Part 314 pertaining to accelerated approval of drugs, 2301 means FDA form for transmittal of periodic reports and promotional material for new animal drugs, 348 means FDA form for sponsored travel, 3500 means FDA form for voluntary reporting of adverse events, 3500A means FDA form for mandatory reporting of adverse events, 356V means FDA form for new animal drug appication, 3R means Recruitment, Relocation bonuses, and Retention allowances, 406B means Section of the FDA Modernization Act dealing with getting feedback from our stakeholders, 482 means FDA form for notice of inspection, 483 means FDA form used as a written notice of deficiencies found in inspections, 505(b)(2) means A new drug application that contains full reports of investigations of safety and effectiveness but , 510(k) means Food, Drug, and Cosmetic Act Section 501(k), Pre-Market Notification, 510(k) means Food, Drug, and Cosmetic Act Section 510(k), Pre-Market Notification, A-V means Arterio-Venous, A-VO2 means Arterio-Venous Oxygen, A/L means Annual Leave, A2LA means American Association for Laboratory Accreditation,

AbbreviationsDefinitionMore
(b)(4)Freedom of Information Act Exemption 4, which protects from disclosure ôtrade secrets and commercial. (b)(4)
1932FDA form for veterinary adverse drug reaction, lack of effectiveness, product defect report--mandatory. 1932
1932aFDA form for veterinary adverse drug reaction, lack of effectiveness, product defect report--voluntary. 1932a
21 CFR Part 314 Subpart HSubpart of Part 314 pertaining to accelerated approval of drugs. 21 CFR Part 314 Subpart H
2301FDA form for transmittal of periodic reports and promotional material for new animal drugs. 2301
348FDA form for sponsored travel. 348
3500FDA form for voluntary reporting of adverse events. 3500
3500AFDA form for mandatory reporting of adverse events. 3500A
356VFDA form for new animal drug appication. 356V
3RRecruitment, Relocation bonuses, and Retention allowances. 3R
406BSection of the FDA Modernization Act dealing with getting feedback from our stakeholders. 406B
482FDA form for notice of inspection. 482
483FDA form used as a written notice of deficiencies found in inspections. 483
505(b)(2)A new drug application that contains full reports of investigations of safety and effectiveness but . 505(b)(2)
510(k)Food, Drug, and Cosmetic Act Section 501(k), Pre-Market Notification. 510(k)
510(k)Food, Drug, and Cosmetic Act Section 510(k), Pre-Market Notification. 510(k)
A-VArterio-Venous. A-V
A-VO2Arterio-Venous Oxygen. A-VO2
A/LAnnual Leave. A/L
A2LAAmerican Association for Laboratory Accreditation. A2LA

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Analytics Big Data Committee
ACCESS
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AIA
Automated Imaging Association
BOSP
Ballard Open Space Plan
BSOI
Block Stochastic Orthononal Iteration