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.
136 related articles for article (PubMed ID: 9537076)
1. [Mutual recognition: experiences and problems in various countries]. Van den Eede C Tijdschr Diergeneeskd; 1998 Jan; 123(2):54-6. PubMed ID: 9537076 [No Abstract] [Full Text] [Related]
2. Implementaton of 'the TSE directive'. Dean S Vet Rec; 2001 May; 148(21):670. PubMed ID: 11400991 [No Abstract] [Full Text] [Related]
3. [The change of the new veterinary drug legislation for delivery of veterinary drugs]. Schutte F Tijdschr Diergeneeskd; 2006 Jan; 131(2):54-5. PubMed ID: 16454094 [No Abstract] [Full Text] [Related]
4. Veterinary pharmacovigilance. Part 1. The legal basis in the European Union. Woodward KN J Vet Pharmacol Ther; 2005 Apr; 28(2):131-47. PubMed ID: 15842304 [TBL] [Abstract][Full Text] [Related]
5. [Change veterinary drug legislation: where are we and what is still to come?]. de Groot H; van Herten J; den Hertog A Tijdschr Diergeneeskd; 2007 Oct; 132(19):752-3. PubMed ID: 17966321 [No Abstract] [Full Text] [Related]
6. Summary of product characteristic: the next step to harmonization registration requirements for veterinary medicinal products in Poland. Sztabińska-Koncka H Regul Toxicol Pharmacol; 2000 Jun; 31(3):311-2. PubMed ID: 10915591 [No Abstract] [Full Text] [Related]
8. [Registration of veterinary drugs: order or chaos?]. Sybesma W Tijdschr Diergeneeskd; 1993 May; 118(9):308-9. PubMed ID: 8488491 [No Abstract] [Full Text] [Related]
9. [Review 2001: The veterinary drug legislation is being revised. A brief insight into the European Union legislation process concerning drugs]. Hulsen J; de Groot H Tijdschr Diergeneeskd; 2003 Sep; 128(17):521-3. PubMed ID: 14582150 [No Abstract] [Full Text] [Related]
10. [The Veterinary Drug Act and the practice for domestic animals]. Takkenberg RJ Tijdschr Diergeneeskd; 1987 Apr; 112(8):478-80. PubMed ID: 3576583 [TBL] [Abstract][Full Text] [Related]
11. [Europe 1993 and drugs]. Reuse J Bull Mem Acad R Med Belg; 1990; 145(8-9):341-9; discussion 349-50. PubMed ID: 2099233 [No Abstract] [Full Text] [Related]
12. [POM]. van den Ekker W Tijdschr Diergeneeskd; 2006 Jul; 131(13):496. PubMed ID: 16866166 [No Abstract] [Full Text] [Related]
13. Pharmacovigilance of veterinary medicines. Jones P; Sundlof SF J Vet Pharmacol Ther; 2005 Apr; 28(2):127-8. PubMed ID: 15842302 [No Abstract] [Full Text] [Related]
14. [IBR control with the European Union]. Batza HJ Tijdschr Diergeneeskd; 1995 Sep; 120(17):501-2. PubMed ID: 7570554 [No Abstract] [Full Text] [Related]
15. [The new veterinary drug agreement and the new veterinary drug rules 2005: what does that mean for your practice?]. de Groot H; van Herten J Tijdschr Diergeneeskd; 2006 Jan; 131(1):14-7. PubMed ID: 16430161 [No Abstract] [Full Text] [Related]
16. International Cooperation on Harmonisation of Technical Requirements for Approval of Veterinary Medicinal Products (VICH); final guidance for industry on "studies to evaluate the safety of residues of veterinary drugs in human food: genotoxicity testing" (VICH GL23); availability. Notice. Food and Drug Administration, HHS Fed Regist; 2002 Jan; 67(3):602-3. PubMed ID: 12358039 [TBL] [Abstract][Full Text] [Related]
17. [The EEC creates a European Medical Product Agency]. Johnson K Lakartidningen; 1993 Oct; 90(40):3395. PubMed ID: 8231477 [No Abstract] [Full Text] [Related]
18. FDA and mutual recognition agreements: five models of harmonization. Merrill RA Food Drug Law J; 1998; 53(1):133-7. PubMed ID: 11795329 [No Abstract] [Full Text] [Related]
19. Assessment of user safety, exposure and risk to veterinary medicinal products in the European Union. Woodward KN Regul Toxicol Pharmacol; 2008 Feb; 50(1):114-28. PubMed ID: 18060673 [TBL] [Abstract][Full Text] [Related]