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Device register
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511	Federal Register / Vol. 77, No[removed]Friday, June 1, [removed]Notices gov/downloads/MedicalDevices/Device RegulationandGuidance/Guidance Documents/UCM080199.pdf or by sending an email request to [removed] to rece Add to Reading List Source URL: oig.hhs.gov Language: English - Date: 2012-06-01 10:32:10 Government Inspectors general Inspector General United States Department of Health and Human Services Medicaid Medicare Federal assistance in the United States Healthcare reform in the United States Presidency of Lyndon B. Johnson
512	3738 Federal Register / Vol. 79, No[removed]Thursday, January 23, [removed]Rules and Regulations Title: FERC–725R, Mandatory Reliability Standards: Reliability Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2014-01-23 02:35:15 Technology Pharmaceuticals policy Food law Pharmaceutical industry Medical equipment Premarket approval Federal Food Drug and Cosmetic Act Medical device Title 21 of the Code of Federal Regulations Medicine Food and Drug Administration Health
513	Federal Register / Vol. 79, No. 7 / Friday, January 10, [removed]Rules and Regulations solely to the agency’s organization, procedure, or practice. Accordingly, the provisions of the Administrative Procedure Act regardin Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2014-01-10 00:30:54 Technology Federal Food Drug and Cosmetic Act Premarket approval Medical device Center for Devices and Radiological Health Humanitarian Device Exemption Title 21 CFR Part 11 Off-label use Food and Drug Administration Medicine Health
514	Federal Register / Vol. 79, No[removed]Wednesday, April 23, [removed]Notices For Public Toll Free Telephone: ([removed]–1088 Participant passcode: [removed]Participant URL: https:// www.mymeetings.com/nc/join/ Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2014-04-23 03:15:06 Food and Drug Administration Food law Food and drink Federal Food Drug and Cosmetic Act Animal drugs Generic drug Title 21 of the Code of Federal Regulations Medical device Food coloring Medicine Health Pharmaceuticals policy
515	TKELLEY on DSK3SPTVN1PROD with NOTICES Federal Register / Vol. 79, No[removed]Thursday, April 17, [removed]Notices labels because they increase the number of label elements that establishments must take into account when de Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2014-04-17 07:08:45 Health Pharmaceuticals policy Paperwork Reduction Act Title 21 of the Code of Federal Regulations Food Safety Modernization Act Medical device Federal Food Drug and Cosmetic Act Medicine Food and Drug Administration Food law
516	tkelley on DSK3SPTVN1PROD with NOTICES Federal Register / Vol. 79, No[removed]Friday, July 11, [removed]Notices Supplements Under GDUFA.’’ The Generic Drug User Fee Amendments of[removed]GDUFA) enables FDA to assess Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2014-07-16 16:29:04 Pharmacology Clinical research Pharmaceuticals policy Abbreviated New Drug Application New Drug Application Generic drug ClinicalTrials.gov Unique Device Identification Pharmaceutical industry Food and Drug Administration Pharmaceutical sciences
517	[removed]Federal Register / Vol. 79, No[removed]Wednesday, April 23, [removed]Notices manufacturer’s batch number is used for temporarily identifying a batch of color additive until FDA issues a certification Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2014-04-23 03:15:06 Technology Food law Pharmaceuticals policy Adulteration Federal Food Drug and Cosmetic Act Premarket approval Medical device Title 21 of the Code of Federal Regulations Center for Devices and Radiological Health Medicine Food and Drug Administration Health
518	Federal Register / Vol. 62, No[removed]Wednesday, April 2, [removed]Notices which uses him in any capacity on PHS supported research must concurrently submit a plan for supervision of his duties. The supervisory plan must be Add to Reading List Source URL: www.fda.gov Language: English Technology Debarment Federal Food Drug and Cosmetic Act New Drug Application Medical device Premarket approval Center for Devices and Radiological Health Title 21 of the Code of Federal Regulations Food and Drug Administration Medicine Health
519	Federal Register / Vol. 63, No[removed]Thursday, June 11, [removed]Notices c. Obtain informed client consent by explaining the risks of disclosure and the recipient’s policies and procedures for preventing unauthorized di Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical sciences Pharmacology Pharmaceuticals policy Debarment United States law Food law Federal Food Drug and Cosmetic Act Premarket approval Medical device Medicine Food and Drug Administration Health
520	Welcome to today’s FDA/CDRH Webinar Thank you for your patience while we register all of today’s participants. If you have not connected to the audio Add to Reading List Source URL: www.fda.gov Language: English Technology Center for Devices and Radiological Health Medical device Premarket approval Food and Drug Administration Medicine Health

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