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Results: 1 to 20 of 120

Similar articles for PubMed (Select 23695480)

1.

Value of unique device identification in the digital health infrastructure.

Wilson NA, Drozda J.

JAMA. 2013 May 22;309(20):2107-8. doi: 10.1001/jama.2013.5514. No abstract available.

PMID:
23695480
2.

Detecting software failures in the MAUDE database: a preliminary analysis.

Pecoraro F, Luzi D.

Stud Health Technol Inform. 2013;192:1098.

PMID:
23920872
3.

Postmarketing surveillance of medical devices--filling in the gaps.

Resnic FS, Normand SL.

N Engl J Med. 2012 Mar 8;366(10):875-7. doi: 10.1056/NEJMp1114865. Epub 2012 Feb 14. No abstract available.

4.

Medical device accident reporting: does it improve patient safety?

Nobel JJ.

Stud Health Technol Inform. 1996;28:29-35.

PMID:
10172828
5.

MedWatch. On lookout for medical product problems.

Ropp KL.

FDA Consum. 1993 Nov;27(9):14-7. No abstract available.

PMID:
10130376
6.

Achieving meaningful device surveillance: from reaction to proaction.

Rumsfeld JS, Peterson ED.

JAMA. 2010 Nov 10;304(18):2065-6. doi: 10.1001/jama.2010.1648. No abstract available.

PMID:
21063018
7.

HomeNet: ensuring patient safety with medical device use in the home.

Kaufman D, Weick-Brady M.

Home Healthc Nurse. 2009 May;27(5):300-7. Review. No abstract available.

PMID:
19448498
8.

MedWatch program.

White GG.

Int J Trauma Nurs. 1998 Jul-Sep;4(3):100-3. No abstract available.

PMID:
9855977
9.

The year 2000 and biomedical equipment.

[No authors listed]

Int J Trauma Nurs. 1998 Oct-Dec;4(4):146-7. No abstract available.

PMID:
9855987
10.

Medical device vigilance at FDA.

Gross TP, Kessler LG.

Stud Health Technol Inform. 1996;28:17-24.

PMID:
10164091
11.

Record linkage for postmarketing surveillance.

Faich GA.

Clin Pharmacol Ther. 1989 Oct;46(4):479-80. No abstract available.

PMID:
2791451
12.

MedWatch: FDA's new medical products reporting program.

Kessler DA, Kennedy DL.

J Clin Eng. 1993 Nov-Dec;18(6):489-92. No abstract available.

PMID:
10130858
13.

Preface to supplement. Active surveillance of vaccine safety in the US Food and Drug Administration's Mini-Sentinel program: identification of exposures and outcomes.

[No authors listed]

Vaccine. 2013 Dec 30;31 Suppl 10:K1. doi: 10.1016/j.vaccine.2013.10.087. No abstract available.

PMID:
24331068
14.

FDA works to reduce preventable medical device injuries.

Rados C.

FDA Consum. 2003 Jul-Aug;37(4):29-33. No abstract available.

15.

Computerized medical device tracking--ways to comply with SMDA (Safe Medical Devices Act of 1990).

Landis D.

Healthc Inform. 1992 Jul;9(7):36, 38, 40-2. No abstract available.

PMID:
10119858
16.

But doctor, it's my hip!: the fate of failed medical devices.

Fielder JH, Black J.

Kennedy Inst Ethics J. 1995 Jun;5(2):113-31. Review.

PMID:
10172331
17.

Medical device reports raise and red flag.

Miles F, Miles JF.

Provider. 1997 Jan;23(1):53, 55-6. No abstract available.

PMID:
10166155
18.

The US Food and Drug Administration's Sentinel Initiative: expanding the horizons of medical product safety.

Robb MA, Racoosin JA, Sherman RE, Gross TP, Ball R, Reichman ME, Midthun K, Woodcock J.

Pharmacoepidemiol Drug Saf. 2012 Jan;21 Suppl 1:9-11. doi: 10.1002/pds.2311. No abstract available.

PMID:
22262587
19.

FDA turns to electronic "sentinel" to flag prescription drug safety problems.

Kuehn BM.

JAMA. 2008 Jul 9;300(2):156-7. doi: 10.1001/jama.300.2.156. No abstract available.

PMID:
18612108
20.

Unique device identification in the service of public health.

Gross TP, Crowley J.

N Engl J Med. 2012 Oct 25;367(17):1583-5. doi: 10.1056/NEJMp1113608. Epub 2012 Sep 26. No abstract available.

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