Combination products neglected by FDA device evaluation.
- Published in:
- Nature Medicine, 2011, v. 17, n. 9, p. 1024, doi. 10.1038/nm0911-1024a
- By:
- Publication type:
- Article
Works matching DE "CENTER for Devices %26 Radiological Health (U.S.)"
Results: 19
1
2
Abstracts.
- Published in:
- Annals of Biomedical Engineering, 2016, v. 44, n. 12, p. 3719, doi. 10.1007/s10439-016-1710-7
- Publication type:
- Article
3
An in silico framework for integrating epidemiologic and genetic evidence with health care applications: ventilation-related pneumothorax as a case illustration.
- Published in:
- 2016
- By:
- Publication type:
- journal article
4
FDA lens-testing rules could have far-reaching effects.
- Published in:
- Ocular Surgery News, 2008, v. 26, n. 4, p. 29
- By:
- Publication type:
- Article
5
Are current regulations for approval of in vitro diagnostic devices adequate?
- Published in:
- 1998
- By:
- Publication type:
- journal article
6
A conversation with Dr. Greg Campbell.
- Published in:
- 2016
- By:
- Publication type:
- Interview
7
Bayesian Approaches in Medical Device Clinical Trials: A Discussion with Examples in the Regulatory Setting.
- Published in:
- Journal of Biopharmaceutical Statistics, 2011, v. 21, n. 5, p. 938, doi. 10.1080/10543406.2011.589650
- By:
- Publication type:
- Article
8
Combination Products Regulation at the FDA.
- Published in:
- Clinical Pharmacology & Therapeutics, 2009, v. 85, n. 5, p. 468, doi. 10.1038/clpt.2009.28
- By:
- Publication type:
- Article
9
The Latest Word.
- Published in:
- Seybold Report: Analyzing Publishing Technologies, 2013, v. 13, n. 6, p. 11
- Publication type:
- Article
10
Hearing voices: FDA seeks advice from patients.
- Published in:
- 2015
- By:
- Publication type:
- Editorial
11
System Changes to Ensure Patient Safety and Access to Innovative Devices.
- Published in:
- MD Conference Express, 2013, p. 32, doi. 10.1177/155989771319017
- By:
- Publication type:
- Article
12
Untitled.
- Published in:
- MD Conference Express, 2013, p. 12
- By:
- Publication type:
- Article
13
Many heparin-flush makers did not need manufacturing inspection.
- Published in:
- American Journal of Health-System Pharmacy, 2008, v. 65, n. 4, p. 280, doi. 10.2146/news080013
- By:
- Publication type:
- Article
14
Limb salvage shunt receives expedited US FDA approval.
- Published in:
- Expert Review of Medical Devices, 2007, v. 4, n. 2, p. 103, doi. 10.1586/17434440.4.2.103
- Publication type:
- Article
15
FDA Ponders Regulation and Innovation.
- Published in:
- JAMA: Journal of the American Medical Association, 2011, v. 305, n. 15, p. 1523, doi. 10.1001/jama.2011.493
- By:
- Publication type:
- Article
16
Working With the Food and Drug Administration's Center for Devices to Advance Regulatory Science and Medical Device Innovation.
- Published in:
- 2015
- By:
- Publication type:
- Editorial
17
Performing clinical studies involving hernia mesh devices: what every investigator should know about the FDA investigational device exemption (IDE) process.
- Published in:
- Hernia, 2011, v. 15, n. 6, p. 603, doi. 10.1007/s10029-011-0872-3
- By:
- Publication type:
- Article
18
Additively manufactured medical products - the FDA perspective.
- Published in:
- 3D Printing in Medicine, 2016, v. 2, n. 1, p. 1, doi. 10.1186/s41205-016-0005-9
- By:
- Publication type:
- Article
19
A regulatory framework emerges for digital medicine.
- Published in:
- Nature Biotechnology, 2015, v. 33, n. 7, p. 697, doi. 10.1038/nbt.3284
- By:
- Publication type:
- Article