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Showing 1 to 12 of 190 entries
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Strategy and planning for chemopreventive drug development: clinical development plans. Chemoprevention Branch and Agent Development Committee. National Cancer Institute.

Journal of cellular biochemistry. Supplement

Kelloff GJ, Crowell JA, Boone CW, Steele VE, Lubet RA, Greenwald P, Alberts DS, Covey JM, Doody LA, Knapp GG.
PMID: 7616753
J Cell Biochem Suppl. 1994;20:55-62. doi: 10.1002/jcb.240560906.

At the National Cancer Institute, Division of Cancer Prevention and Control, the Chemoprevention Branch and Agent Development Committee develop strategies for efficiently identifying, procuring, and advancing the most promising drugs into clinical trials. Scientific expertise is applied at each...

[Direct research on the development of new drugs from Chinese composite recipes].

Zhongguo Zhong xi yi jie he za zhi Zhongguo Zhongxiyi jiehe zazhi = Chinese journal of integrated traditional and Western medicine

Du L, Yang S, Xu L.
PMID: 11789178
Zhongguo Zhong Xi Yi Jie He Za Zhi. 2000 Sep;20(9):698-9.

No abstract available.

An e-mail system for obtaining approval to use a restricted agent.

American journal of health-system pharmacy : AJHP : official journal of the American Society of Health-System Pharmacists

Conlin PR, Alexis G.
PMID: 10613371
Am J Health Syst Pharm. 1999 Dec 15;56(24):2535-7. doi: 10.1093/ajhp/56.24.2535.

Because of concerns over cost, proper patient selection, and prescribing patterns, pharmacy and therapeutics committees must be very selective about which new medications can be added to formularies and used in health systems. However, in the final analysis, many...

Recap of FDA product approvals--2000.

American journal of health-system pharmacy : AJHP : official journal of the American Society of Health-System Pharmacists

Traynor K.
PMID: 11258167
Am J Health Syst Pharm. 2001 Mar 01;58(5):363, 366-8.

No abstract available.

FDA consolidates review process for new pharmaceuticals.

FDA consumer

[No authors listed]
PMID: 12523280
FDA Consum. 2002 Nov-Dec;36(6):2.

No abstract available.

The numbers game.

Nature reviews. Drug discovery

[No authors listed]
PMID: 12474850
Nat Rev Drug Discov. 2002 Dec;1(12):929. doi: 10.1038/nrd983.

No abstract available.

FDA publishes analysis of the pipeline problem.

Nature reviews. Drug discovery

Frantz S.
PMID: 15152628
Nat Rev Drug Discov. 2004 May;3(5):379. doi: 10.1038/nrd1404.

No abstract available.

Panel eases US drug approval process.

The Lancet. Oncology

Susman E.
PMID: 14974474
Lancet Oncol. 2004 Feb;5(2):71. doi: 10.1016/s1470-2045(04)01367-1.

No abstract available.

Pharmaceutical research and development.

Clinical therapeutics

McKercher PL.
PMID: 1468093
Clin Ther. 1992 Sep-Oct;14(5):760-4; discussion 759.

Some aspects of pharmaceutical research and development (R&D) are reviewed. The viability of major pharmaceutical manufacturers depends on their research and thus they commit substantial resources to R&D programs. Major pharmaceutical manufacturers in the United States employ about 40,000...

Drug delay and the FDA.

International journal of dermatology

Barranco VP.
PMID: 1399193
Int J Dermatol. 1992 Oct;31(10):691-2. doi: 10.1111/j.1365-4362.1992.tb01372.x.

No abstract available.

FDA clears 26 new drugs for marketing in 1992.

American journal of hospital pharmacy

[No authors listed]
PMID: 8470670
Am J Hosp Pharm. 1993 Apr;50(4):578, 581.

No abstract available.

New Drugs Approved in 2019.

The American journal of medicine

Ebied AM, Patel KH, Cooper-DeHoff RM.
PMID: 32145207
Am J Med. 2020 Jun;133(6):675-678. doi: 10.1016/j.amjmed.2020.01.030. Epub 2020 Mar 05.

In 2019, the US Food and Drug Administration (FDA) approved 48 novel drugs. Thirty of the 48 (62.5%) novel drug approvals were reviewed and approved through an expedited review pathway while 20 of the 48 (41.7%) were approved for...

Showing 1 to 12 of 190 entries