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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1938 1
1945 3
1946 1
1947 4
1948 2
1949 6
1953 2
1954 2
1955 4
1956 18
1957 6
1958 1
1959 3
1960 4
1961 6
1962 1
1963 5
1964 29
1965 44
1966 66
1967 69
1968 90
1969 85
1970 125
1971 110
1972 150
1973 184
1974 226
1975 198
1976 199
1977 203
1978 330
1979 343
1980 286
1981 192
1982 228
1983 231
1984 233
1985 304
1986 271
1987 348
1988 485
1989 568
1990 602
1991 745
1992 860
1993 926
1994 892
1995 1078
1996 1229
1997 1216
1998 1430
1999 1369
2000 1391
2001 1476
2002 1602
2003 1630
2004 2004
2005 1880
2006 2167
2007 2280
2008 2319
2009 2369
2010 2733
2011 3004
2012 3300
2013 3427
2014 3808
2015 4035
2016 4361
2017 4794
2018 5136
2019 5106
2020 5767
2021 6126
2022 5777
2023 5612
2024 2930

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92,786 results

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Page 1
The Food and Drug Administration's Role in Dermatologic Drug Development.
Lewis FS, Marcus KA. Lewis FS, et al. Dermatol Clin. 2022 Jul;40(3):249-263. doi: 10.1016/j.det.2022.02.001. Dermatol Clin. 2022. PMID: 35750409 Review.
The mission of the Food and Drug Administration (FDA) is to ensure the safety and effectiveness of dermatologic drugs, as authorized by the Federal Food, Drug, and Cosmetic Act (FD&CA). ...
The mission of the Food and Drug Administration (FDA) is to ensure the safety and effectiveness of dermatologic …
The History of Dermatology and Dermatologists at the US Food and Drug Administration.
Burrows VL, Luke MC. Burrows VL, et al. Dermatol Clin. 2022 Jul;40(3):237-248. doi: 10.1016/j.det.2022.03.001. Dermatol Clin. 2022. PMID: 35750408 Review.
In the United States, the Food and Drug Administration's (FDA's) regulatory authorities have significantly influenced the products available to treat dermatologic conditions, but at the same time, advances in dermatology have also influenced the FDA's …
In the United States, the Food and Drug Administration's (FDA's) regulatory authorities have significantly influ …
United States Food and Drug Administration Regulation of Human Cells, Tissues, and Gene Therapies.
Sanduja S, Lessey-Morillon L, Allen R, Wang X, Imperato G, Arcidiacono J. Sanduja S, et al. Adv Exp Med Biol. 2023;1430:71-89. doi: 10.1007/978-3-031-34567-8_5. Adv Exp Med Biol. 2023. PMID: 37526843 Review.
The Office of Therapeutic Products (OTP) in the Center for Biologics Evaluation and Research (CBER) at the United States Food and Drug Administration (US FDA) is responsible for the regulation of these products, among others, throughout the entire prod …
The Office of Therapeutic Products (OTP) in the Center for Biologics Evaluation and Research (CBER) at the United States Food and …
Food and Drug Administration.
Horton LR. Horton LR. BMJ. 2007 Jan 13;334(7584):55-6. doi: 10.1136/bmj.39049.545880.BE. BMJ. 2007. PMID: 17218671 Free PMC article.
Demystifying the U.S. Food and Drug Administration: understanding regulatory pathways.
Naghshineh N, Brown S, Cederna PS, Levi B, Lisiecki J, D'Amico RA, Hume KM, Seward W, Rubin JP. Naghshineh N, et al. Plast Reconstr Surg. 2014 Sep;134(3):559-569. doi: 10.1097/PRS.0000000000000477. Plast Reconstr Surg. 2014. PMID: 25158712 Review.
Food and Drug Administration perplexing, overly complicated, and insurmountable. The authors aim to clearly outline the path of the regulatory process as it pertains to the U.S. Food and Drug Administration and its various j …
Food and Drug Administration perplexing, overly complicated, and insurmountable. The authors aim to clearly outl …
Review of novel and supplemental approvals of the targeted cancer drugs by the Food and Drug Administration in 2021.
Kandemir EA. Kandemir EA. J Oncol Pharm Pract. 2023 Jan;29(1):191-207. doi: 10.1177/10781552221112015. Epub 2022 Jul 6. J Oncol Pharm Pract. 2023. PMID: 35793068 Review.
OBJECTIVE: This review aims to present the most recent results from clinical trials of targeted cancer drugs that led to the Food and Drug Administration approval in 2021 and reflect the changing treatment landscape of solid malignancies. ...DATA SUMMA …
OBJECTIVE: This review aims to present the most recent results from clinical trials of targeted cancer drugs that led to the Food …
Recent Actions by the US Food and Drug Administration: Reducing the Risk of Infection from Reprocessed Duodenoscopes.
Haugen SP, Ferriter A, Connell J, Min LJ, Wiyor HD, Cole S. Haugen SP, et al. Gastrointest Endosc Clin N Am. 2020 Oct;30(4):711-721. doi: 10.1016/j.giec.2020.06.010. Epub 2020 Jul 30. Gastrointest Endosc Clin N Am. 2020. PMID: 32891227 Review.
Such a community can raise awareness of the importance of duodenoscope cleaning, work to improve reprocessing training, identify the most pressing unanswered questions that merit further research, and develop tools that can be used by health care facilities to improve the quality …
Such a community can raise awareness of the importance of duodenoscope cleaning, work to improve reprocessing training, identify the most pr …
[The role of the Food and Drug Administration as times change].
Keiding N. Keiding N. Ugeskr Laeger. 2018 May 7;180(19):V11170868. Ugeskr Laeger. 2018. PMID: 29761775 Free article. Review. Danish.
The prestigious journal Biostatistics published in July 2017 six solicited commentaries on the role of the U.S. Food and Drug Administration (FDA), as times change, with ever developing technical tools for clinical trials and their evaluation, with inc …
The prestigious journal Biostatistics published in July 2017 six solicited commentaries on the role of the U.S. Food and Dr …
Consequences of the U.S. Food and Drug Administration-Directed Moratorium on Silicone Gel Breast Implants: 1992 to 2006.
Cole NM. Cole NM. Plast Reconstr Surg. 2018 May;141(5):1137-1141. doi: 10.1097/PRS.0000000000004284. Plast Reconstr Surg. 2018. PMID: 29697610 Review.
The U.S. Food and Drug Administration silicone gel breast implant moratorium occurred 25 years ago. ...
The U.S. Food and Drug Administration silicone gel breast implant moratorium occurred 25 years ago. ...
92,786 results
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