These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

121 related articles for article (PubMed ID: 7748605)

  • 21. FDA's priority-based assessment of food additives. II. General toxicity parameters.
    Rulis AM; Hattan DG
    Regul Toxicol Pharmacol; 1985 Jun; 5(2):152-74. PubMed ID: 3839589
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Trends of FDA resource allocations over the past 20 years: expected future resources and workload.
    Shank FR; Bailey CJ
    Regul Toxicol Pharmacol; 1996 Dec; 24(3):218-23. PubMed ID: 8975748
    [No Abstract]   [Full Text] [Related]  

  • 23. Data gaps in toxicity testing of chemicals allowed in food in the United States.
    Neltner TG; Alger HM; Leonard JE; Maffini MV
    Reprod Toxicol; 2013 Dec; 42():85-94. PubMed ID: 23954440
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Food and Drug Administration Proposed Guidelines for Neurotoxicological Testing of Food Chemicals.
    Sobotka TJ; Ekelman KB; Slikker W; Raffaele K; Hattan DG
    Neurotoxicology; 1996; 17(3-4):825-36. PubMed ID: 9086506
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Food and Drug Administration: approach to evaluating neurotoxicity.
    Sobotka TJ
    Toxicol Ind Health; 1989 Mar; 5(2):157-64. PubMed ID: 2728012
    [TBL] [Abstract][Full Text] [Related]  

  • 26. FDA'S food ingredient approval process: Safety assurance based on scientific assessment.
    Rulis AM; Levitt JA
    Regul Toxicol Pharmacol; 2009 Feb; 53(1):20-31. PubMed ID: 18983884
    [TBL] [Abstract][Full Text] [Related]  

  • 27. What are additives?
    Zivković R
    Acta Med Croatica; 2001; 55(4-5):203-6. PubMed ID: 12398024
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Under the law, FDA must grant different standards for new dietary ingredients and food additives.
    Mister S; Hathcock J
    Regul Toxicol Pharmacol; 2012 Apr; 62(3):456-8. PubMed ID: 22310217
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Nanotherapeutics--product development along the "nanomaterial" discussion.
    Wacker MG
    J Pharm Sci; 2014 Mar; 103(3):777-84. PubMed ID: 24481705
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Launching a new food product or dietary supplement in the United States: industrial, regulatory, and nutritional considerations.
    Finley JW; Finley JW; Ellwood K; Hoadley J
    Annu Rev Nutr; 2014; 34():421-47. PubMed ID: 24850389
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Conflicts of interest in approvals of additives to food determined to be generally recognized as safe: out of balance.
    Neltner TG; Alger HM; O'Reilly JT; Krimsky S; Bero LA; Maffini MV
    JAMA Intern Med; 2013 Dec 9-23; 173(22):2032-6. PubMed ID: 23925593
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Food ingredient review at FDA: recent data and initiatives to improve the process.
    Rulis AM; Tarantino LM
    Regul Toxicol Pharmacol; 1996 Dec; 24(3):224-31. PubMed ID: 8975749
    [No Abstract]   [Full Text] [Related]  

  • 33. Qualitative identification of permitted and non-permitted colour additives in food products.
    Harp BP; Miranda-Bermudez E; Baron CI; Richard GI
    Food Addit Contam Part A Chem Anal Control Expo Risk Assess; 2012; 29(6):886-96. PubMed ID: 22540286
    [TBL] [Abstract][Full Text] [Related]  

  • 34. FDA clarifies policy on salmonellae in feed, holds workshop on anti-Salmonella additives.
    J Am Vet Med Assoc; 1994 Oct; 205(8):1088. PubMed ID: 7890561
    [No Abstract]   [Full Text] [Related]  

  • 35. The safety of ethyl oleate is supported by a 91-day feeding study in rats.
    Bookstaff RC; Stuard SB; Ward SR; Pesik PK; Henwood SM
    Regul Toxicol Pharmacol; 2004 Apr; 39(2):202-13. PubMed ID: 15041149
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Safety standards in infant nutrition: a United States perspective.
    Bier DM
    Ann Nutr Metab; 2012; 60(3):192-5. PubMed ID: 22699766
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Draft guidance for industry; exports and imports under the FDA Export Reform and Enhancement Act of 1996--FDA. Notice.
    Fed Regist; 1998 Jun; 63(113):32219-34. PubMed ID: 10180275
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Safety assurance margins for food additives currently in use.
    Rulis AM
    Regul Toxicol Pharmacol; 1987 Jun; 7(2):160-8. PubMed ID: 3303168
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Comparison of two guidelines on immunotoxicity testing of medicinal products.
    Dujmović IH
    Arh Hig Rada Toksikol; 2005 Sep; 56(3):265-8. PubMed ID: 16180612
    [TBL] [Abstract][Full Text] [Related]  

  • 40. FDA toxicity databases and real-time data entry.
    Arvidson KB
    Toxicol Appl Pharmacol; 2008 Nov; 233(1):17-9. PubMed ID: 18656494
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.