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Journal Abstract Search
336 related items for PubMed ID: 10156421
1. Deterring inefficient pharmaceutical litigation: an economic rationale for the FDA regulatory compliance defense. Viscusi WK, Rowland SR, Dorfman HL, Walsh CJ. Spec Law Dig Health Care Law; 1996 Mar; (205):9-52. PubMed ID: 10156421 [No Abstract] [Full Text] [Related]
2. Informed by the European Union experience: what the United States can anticipate and learn from the European Union's regulatory approach to biosimilars. Gitter DM. Seton Hall Law Rev; 2011 Mar; 41(2):559-92. PubMed ID: 21739759 [No Abstract] [Full Text] [Related]
3. FDA cracks down on labeling, initiates trial result reporting. Osborne R, Waltz E. Nat Biotechnol; 2008 Nov; 26(11):1203-4. PubMed ID: 18997742 [No Abstract] [Full Text] [Related]
4. Pediatric testing of prescription drugs: the Food and Drug Administration's carrot and stick for the pharmaceutical industry. Karst KR. Am Univ Law Rev; 2000 Nov; 49():739-72. PubMed ID: 11067732 [No Abstract] [Full Text] [Related]
5. The federal preemption debate in pharmaceutical labeling product liability actions. Gross JM, Curry JA. Tort Trial Insur Pract Law J; 2007 Nov; 43(1):35-70. PubMed ID: 18354866 [No Abstract] [Full Text] [Related]
6. US lawmakers tackle safety reforms at the FDA. Zwillich T. Lancet; 2007 Jun 16; 369(9578):1989-90. PubMed ID: 17577942 [No Abstract] [Full Text] [Related]
7. Bolstering the FDA's drug-safety authority. Schultz WB. N Engl J Med; 2007 Nov 29; 357(22):2217-9. PubMed ID: 18046024 [No Abstract] [Full Text] [Related]
8. Pin the tail on the other donkey: allocating and avoiding injury losses after drug or device approval. O'Reilly JT. Food Drug Law J; 2007 Nov 29; 62(3):559-72. PubMed ID: 17915397 [No Abstract] [Full Text] [Related]
9. FDA prohibits extralabel use of two drug classes. J Am Vet Med Assoc; 1997 Aug 01; 211(3):269. PubMed ID: 9262656 [No Abstract] [Full Text] [Related]
10. FDA attempting to overcome major roadblocks in monitoring drug safety. Zielinski SL. J Natl Cancer Inst; 2005 Jun 15; 97(12):872-3. PubMed ID: 15956645 [No Abstract] [Full Text] [Related]
11. Accelerated approval of oncology products: the food and drug administration experience. Johnson JR, Ning YM, Farrell A, Justice R, Keegan P, Pazdur R. J Natl Cancer Inst; 2011 Apr 20; 103(8):636-44. PubMed ID: 21422403 [Abstract] [Full Text] [Related]
12. PLIVA v. Mensing: generic consumers' unfortunate hand. Lee SB. Yale J Health Policy Law Ethics; 2012 Apr 20; 12(2):209-63. PubMed ID: 23175916 [No Abstract] [Full Text] [Related]
13. FDA perspectives on supplement use by patients on antithrombotic therapy: dietary supplement regulatory overview. Woo JJ. Thromb Res; 2005 Apr 20; 117(1-2):193-6; discussion 201-7. PubMed ID: 16253311 [No Abstract] [Full Text] [Related]
14. Legal implications of pharmacogenomics regarding drug trials, drug labeling, and genetic testing for drug prescription: an international approach. Mandry T. Food Drug Law J; 2004 Apr 20; 59(4):519-35. PubMed ID: 15875348 [Abstract] [Full Text] [Related]
16. FDA regulatory compliance reconsidered. Tobias C. Cornell Law Rev; 2008 Jul 20; 93(5):1003-38. PubMed ID: 18618969 [No Abstract] [Full Text] [Related]
17. Regulatory considerations for determining postmarketing study commitments. Meyer RJ. Clin Pharmacol Ther; 2007 Aug 20; 82(2):228-30. PubMed ID: 17538552 [Abstract] [Full Text] [Related]
18. Postmarketing surveillance for oncology drugs. Viale PH, Moore S. Clin J Oncol Nurs; 2008 Dec 20; 12(6):877-86. PubMed ID: 19064381 [Abstract] [Full Text] [Related]
19. Prescription for trouble: common drugs, hidden dangers. Tens of people are at risk. Consum Rep; 2006 Jan 20; 71(1):34-9. PubMed ID: 16491527 [No Abstract] [Full Text] [Related]
20. FDA Modernization Act: implications for oncology. Morris L. Oncology (Williston Park); 1998 Nov 20; 12(11A):139-41. PubMed ID: 10028506 [Abstract] [Full Text] [Related] Page: [Next] [New Search]