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Journal Abstract Search
267 related items for PubMed ID: 8361258
1. The development of good clinical practice in the EEC and in Germany. Anhalt E. Methods Find Exp Clin Pharmacol; 1993 May; 15(4):217-22. PubMed ID: 8361258 [Abstract] [Full Text] [Related]
4. Inspection of clinical investigations by the German health authorities. Schmidt M. Methods Find Exp Clin Pharmacol; 1993 May; 15(4):229-31. PubMed ID: 8361260 [Abstract] [Full Text] [Related]
5. [Community requirements relating to drugs derived from human blood and plasma]. Brunko P. Ann Pharm Fr; 1994 May; 52(2):89-98. PubMed ID: 7944184 [Abstract] [Full Text] [Related]
12. [Harmonisation of regulatory requirements for clinical trials on medicinal products for human use in the Directive 2001/20/EC and complementary guidance. Implementation of the 12th Law Amending the German Drug Law]. Geisler I, Hofmann HP, Nickel L. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz; 2005 Feb; 48(2):141-6. PubMed ID: 15726454 [Abstract] [Full Text] [Related]
18. [The role of ethical committees in drug trials performed according to "Good Clinical Practice"]. Kerpel-Fronius S. Orv Hetil; 1991 Mar 31; 132(13):703-5. PubMed ID: 2014128 [Abstract] [Full Text] [Related]