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Journal Abstract Search
540 related items for PubMed ID: 11993366
1. A critical tipping point. Zuckerman MB. US News World Rep; 2002 Apr 22; 132(13):72. PubMed ID: 11993366 [No Abstract] [Full Text] [Related]
2. The FDA's drug review process: ensuring drugs are safe and effective. Meadows M. FDA Consum; 2002 Apr 22; 36(4):19-24. PubMed ID: 12184298 [No Abstract] [Full Text] [Related]
6. FDA and EMEA pool scientific advice. Katsnelson A. Nat Biotechnol; 2004 Dec 22; 22(12):1490-1. PubMed ID: 15583642 [No Abstract] [Full Text] [Related]
7. Balancing US patent and FDA approval processes: strategically optimizing market exclusivity. Fernandez DS, Huie JT. Drug Discov Today; 2004 Jun 15; 9(12):509-12. PubMed ID: 15183155 [No Abstract] [Full Text] [Related]
8. The big gap at the FDA. Stipp D. Fortune; 2002 Jul 22; 146(2):113-4, 116. PubMed ID: 12141178 [No Abstract] [Full Text] [Related]
9. What ails the FDA? Okie S. N Engl J Med; 2005 Mar 17; 352(11):1063-6. PubMed ID: 15784660 [No Abstract] [Full Text] [Related]
10. Drugs with breakthrough status charm investors. Senior M. Nat Biotechnol; 2013 Nov 17; 31(11):945-7. PubMed ID: 24213748 [No Abstract] [Full Text] [Related]
11. The Prescription Drug User Fee Act of 1992: speeding up the drug approval process. Bierut MB. Healthspan; 1992 Dec 17; 9(11):12-4. PubMed ID: 10123552 [No Abstract] [Full Text] [Related]
12. BIO and biogenerics. Feldbaum CB. Nat Biotechnol; 2005 Jan 17; 23(1):17; discussion 17. PubMed ID: 15637607 [No Abstract] [Full Text] [Related]
13. Trials and error. Jacobs T. Nat Biotechnol; 2005 Dec 17; 23(12):1481. PubMed ID: 16333284 [No Abstract] [Full Text] [Related]
14. The special treatment. Osborne R. Nat Biotechnol; 2008 May 17; 26(5):487-9. PubMed ID: 18464770 [No Abstract] [Full Text] [Related]
15. Steve Carney talks to Vincent Lee on the pharma industry, the FDA and public education with respect to drugs and their development. Lee VH. Drug Discov Today; 2005 Nov 01; 10(21):1411-4. PubMed ID: 16243258 [No Abstract] [Full Text] [Related]
16. The drive to reform the FDA gains momentum. Gatty B. Hosp Formul; 1995 Mar 01; 30(3):178, 177. PubMed ID: 10141250 [No Abstract] [Full Text] [Related]
17. Maine law requires drug companies to provide clinical trial data. Appell D. J Natl Cancer Inst; 2005 Sep 07; 97(17):1246. PubMed ID: 16145043 [No Abstract] [Full Text] [Related]
18. The Prescription Drug User Fee Act: is a faster Food and Drug Administration always a better Food and Drug Administration? Zelenay JL. Food Drug Law J; 2005 Sep 07; 60(2):261-338. PubMed ID: 16094773 [No Abstract] [Full Text] [Related]
19. Drive for drugs leads to baby clinical trials. Nature; 2006 Mar 23; 440(7083):406-7. PubMed ID: 16554774 [No Abstract] [Full Text] [Related]
20. Who would approve new drugs if there were no FDA? Gatty B. Hosp Formul; 1995 Jan 23; 30(1):58, 57. PubMed ID: 10139726 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]