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 *

178 related articles for article (PubMed ID: 11988365)

  • 1. European medicines and feed additives regulation are not in compliance with environmental legislation and policy.
    Montforts MH; de Knecht JA
    Toxicol Lett; 2002 May; 131(1-2):125-36. PubMed ID: 11988365
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Environmental risk assessment of veterinary pharmaceuticals in the EU: reply to Montforts and de Knecht.
    Long C; Crane M
    Toxicol Lett; 2003 May; 142(3):219-25. PubMed ID: 12691715
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Environmental risk assessment of veterinary medicinal products in the EU--a regulatory perspective.
    Koschorreck J; Koch C; Rönnefahrt I
    Toxicol Lett; 2002 May; 131(1-2):117-24. PubMed ID: 11988364
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Environmental risk assessment for new human pharmaceuticals in the European Union according to the draft guideline/discussion paper of January 2001.
    Straub JO
    Toxicol Lett; 2002 May; 131(1-2):137-43. PubMed ID: 11988366
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Environmental risk assessment for new human pharmaceuticals in the European Union according to the draft guideline/discussion paper of January 2001.
    Straub JO
    Toxicol Lett; 2002 Oct; 135(3):231-7. PubMed ID: 12270681
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A review of the work of the EU Reference Laboratory supporting the authorisation process of feed additives in the EU. [corrected].
    von Holst C; Robouch P; Bellorini S; González de la Huebra MJ; Ezerskis Z
    Food Addit Contam Part A Chem Anal Control Expo Risk Assess; 2016; 33(1):66-77. PubMed ID: 26540604
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Fighting trafficking of falsified and substandard medicinal products in Russia.
    Fayzrakhmanov NF
    Int J Risk Saf Med; 2015; 27 Suppl 1():S37-40. PubMed ID: 26639702
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Strengthening and rationalizing pharmacovigilance in the EU: where is Europe heading to? A review of the new EU legislation on pharmacovigilance.
    Borg JJ; Aislaitner G; Pirozynski M; Mifsud S
    Drug Saf; 2011 Mar; 34(3):187-97. PubMed ID: 21332243
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Review: In vivo and postmortem effects of feed antioxidants in livestock: a review of the implications on authorization of antioxidant feed additives.
    Salami SA; Guinguina A; Agboola JO; Omede AA; Agbonlahor EM; Tayyab U
    Animal; 2016 Aug; 10(8):1375-90. PubMed ID: 26763743
    [TBL] [Abstract][Full Text] [Related]  

  • 10. PBT assessment using the revised annex XIII of REACH: a comparison with other regulatory frameworks.
    Moermond CT; Janssen MP; de Knecht JA; Montforts MH; Peijnenburg WJ; Zweers PG; Sijm DT
    Integr Environ Assess Manag; 2012 Apr; 8(2):359-71. PubMed ID: 22006646
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [EEC regulations for the evaluation of veterinary drugs].
    Bel MN
    Food Addit Contam; 1984; 1(2):205-11. PubMed ID: 6536532
    [No Abstract]   [Full Text] [Related]  

  • 12. Legal constraints in EU product labelling to mitigate the environmental risk of veterinary medicines at use.
    Montforts MH; van Rijswick HF; de Haes HA
    Regul Toxicol Pharmacol; 2004 Dec; 40(3):327-35. PubMed ID: 15546687
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The legal framework governing the quality of (traditional) herbal medicinal products in the European Union.
    Kroes BH
    J Ethnopharmacol; 2014 Dec; 158 Pt B():449-53. PubMed ID: 25086408
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Toward the definition of specific protection goals for the environmental risk assessment of chemicals: A perspective on environmental regulation in Europe.
    Brown AR; Whale G; Jackson M; Marshall S; Hamer M; Solga A; Kabouw P; Galay-Burgos M; Woods R; Nadzialek S; Maltby L
    Integr Environ Assess Manag; 2017 Jan; 13(1):17-37. PubMed ID: 27243906
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Animal health in the European Economic Community. Legislation concerning animal feeds and animal feed additives].
    Ferrando R
    Br Vet J; 1974; 130(6):517-21. PubMed ID: 4447870
    [No Abstract]   [Full Text] [Related]  

  • 16. European legislation for veterinary medicines: Would a monograph system improve the environmental risk assessment?
    de la Casa-Resino I; Haro Castuera A; Casimiro Elena R; Rubio Montejano C; Carapeto García R
    Integr Environ Assess Manag; 2021 Nov; 17(6):1274-1285. PubMed ID: 33913607
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Guarantee of drug quality for animal health and consumer protection].
    Kroker R
    Dtsch Tierarztl Wochenschr; 1994 Jul; 101(7):278-80. PubMed ID: 7924965
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Regulatory aspects of biotechnology in Europe, with particular reference to veterinary science.
    Cantley MF
    Rev Sci Tech; 1990 Sep; 9(3):695-713. PubMed ID: 2132700
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification, assessment and management of "endocrine disruptors" in wildlife in the EU substance legislation--discussion paper from the German Federal Environment Agency (UBA).
    Frische T; Bachmann J; Frein D; Juffernholz T; Kehrer A; Klein A; Maack G; Stock F; Stolzenberg HC; Thierbach C; Walter-Rohde S
    Toxicol Lett; 2013 Dec; 223(3):306-9. PubMed ID: 23500481
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Procedures and methods of benefit assessments for medicines in Germany].
    Bekkering GE; Kleijnen J
    Dtsch Med Wochenschr; 2008 Dec; 133 Suppl 7():S225-46. PubMed ID: 19034813
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.