Works matching DE "MEDICAL equipment safety regulations"

Results: 79

An Innovation to Address a Health Concern is Now a Concern?

Published in:

Performance Improvement, 2018, v. 57, n. 10, p. 45, doi. 10.1002/pfi.21829

By:

Roy, Ria

Publication type:

Article

A better process for new medical devices.

Published in:

2011

By:

Shuren, Jeffrey;
Rosen, Charles;
Young, James B.

Publication type:

Opinion

The Medical Waste Revolution Is on the Horizon:Part II.

Published in:

ONS News, 2004, v. 19, n. 5, p. 10

By:

Biedrzycki, Barbara A.

Publication type:

Article

FDA Requires Bar Codes on Medical Products.

Published in:: ONS News, 2004, v. 19, n. 5, p. 9
Publication type:: Article

Plant Inspections Lag.

Published in:

JAMA: Journal of the American Medical Association, 2008, v. 299, n. 10, p. 1124, doi. 10.1001/jama.299.10.1124-a

By:

Mitka, Mike

Publication type:

Article

SUBSTANTIALLY UNEQUIVALENT: REFORMING FDA REGULATION OF MEDICAL DEVICES.

Published in:

University of Illinois Law Review, 2014, v. 2014, n. 4, p. 1363

By:

LENNOX, KYLE

Publication type:

Article

Perfusion safety: defining the problem.

Published in:

Perfusion, 2005, v. 20, n. 4, p. 195, doi. 10.1191/0267659105pf806oa

By:

Palanzo, David A.

Publication type:

Article

Standards update on perfusion equipment and practice.

Published in:

Perfusion, 2005, v. 20, n. 4, p. 205, doi. 10.1191/0267659105pf808oa

By:

Kurusz, Mark

Publication type:

Article

Die Laborverantwortung für die Sicherheit und Leistung der Prothetik: Aktuelle EU-MDR-Regularien zu ausgelagerten Prozessen bei Sonderanfertigungen.

Published in:

Quintessenz der Zahntechnik, 2022, v. 48, n. 6, p. 604

By:

STOK, ARJAN J. H.

Publication type:

Article

MDR für die Zahntechnik: Die grundlegenden Sicherheits- und Leistungsanforderungen (GruSuLa).

Published in:

Quintessenz der Zahntechnik, 2022, v. 48, n. 6, p. 594

By:

STRIETZEL, ROLAND

Publication type:

Article

Normen: Grundlegende Anforderungen an Medizinprodukte im Rahmen der Medizinprodukteverordnung (MDR).

Published in:

Quintessenz der Zahntechnik, 2021, v. 47, n. 10, p. 1200

By:

STRIETZEL, ROLAND

Publication type:

Article

Postmarket Surveillance of Medical Devices: A Comparison of Strategies in the US, EU, Japan, and China.

Published in:

PLoS Medicine, 2013, v. 10, n. 9, p. 1, doi. 10.1371/journal.pmed.1001519

By:

Kramer, Daniel B.;
Tan, Yongtian T.;
Sato, Chiaki;
Kesselheim, Aaron S.

Publication type:

Article

Negotiating Risk.

Published in:

Technology & Culture, 2013, v. 54, n. 1, p. 1, doi. 10.1353/tech.2013.0022

By:

McKELLAR, SHELLEY

Publication type:

Article

PRINTING FOR THE PERFECT FIT: BALANCING FDA REGULATION OF 3D PRINTED MEDICAL DEVICES.

Published in:

Wisconsin Law Review, 2019, v. 2019, n. 3, p. 593

By:

DYKEMA, RACHEL

Publication type:

Article

Regulation of Medical Devices and Organizational Behavior in Hospitals.

Published in:

Administrative Science Quarterly, 1977, v. 22, n. 3, p. 475, doi. 10.2307/2392184

By:

McNeil, Kenneth;
Minihan, Edmond

Publication type:

Article

Reinventing regulations.

Published in:

JAMA: Journal of the American Medical Association, 1995, v. 273, n. 16, p. 1249, doi. 10.1001/jama.1995.03520400019014

By:

Voelker, Rebecca

Publication type:

Article

Device-specific risk of needlestick injury in Italian health care workers.

Published in:

JAMA: Journal of the American Medical Association, 1994, v. 272, n. 8, p. 607, doi. 10.1001/jama.1994.03520080049042

By:

Ippolito, Giuseppe;
De Carli, Gabriella

Publication type:

Article

Device `fast track' plan.

Published in:

JAMA: Journal of the American Medical Association, 1993, v. 270, n. 6, p. 693, doi. 10.1001/jama.1993.03510060031010

By:

Nightiangle, Stuart L.

Publication type:

Article

Medical Device Regulation: An Introduction for the Practicing Physician.

Published in:

Annals of Internal Medicine, 2004, v. 140, n. 4, p. 296, doi. 10.7326/0003-4819-140-4-200402170-00012

By:

Maisel, William H.

Publication type:

Article

CHALLENGES IN THE EVALUATION OF SAFETY AND EFFICACY OF HUMAN TISSUE AND CELL BASED PRODUCTS.

Published in:

ANZ Journal of Surgery, 2006, v. 76, n. 9, p. 843, doi. 10.1111/j.1445-2197.2006.03880.x

By:

Zheng, Ming H.;
Pembrey, Richard;
Niutta, Silvana;
Stewart-Richardson, Patricia;
Farrugia, Albert

Publication type:

Article

Sixteen‐Hour Ex Vivo Donor Heart Perfusion During Long‐Distance Transportation for Heart Transplantation.

Published in:

2019

By:

Kaliyev, Rymbay;
Bekbossynov, Serik;
Nurmykhametova, Zhuldyz

Publication type:

Case Study

US Health Regulator Issues New Cleaning Guide for Superbug-Prone Device.

Published in:: Clinical Infectious Diseases, 2015, v. 61, n. 8, p. ii, doi. 10.1093/cid/civ753
Publication type:: Article

Tissue Engineering and Regenerative Medicine: Role of Toxicologic Pathologists for an Emerging Medical Technology.

Published in:

Toxicologic Pathology, 2008, v. 36, n. 1, p. 92, doi. 10.1177/0192623307311405

By:

JAYO, MANUEL J.;
WATSON, DAVID D.;
WAGNER, BELINDA J.;
BERTRAM, TIMOTHY A.

Publication type:

Article

Medical Device Regulations and Testing for Toxicologic Pathologists.

Published in:

Toxicologic Pathology, 2008, v. 36, n. 1, p. 63, doi. 10.1177/0192623307309926

By:

SCHUH, JOANN C. L.

Publication type:

Article

Current Status of the Regulation for Medical Devices.

Published in:

Indian Journal of Pharmaceutical Sciences, 2008, v. 70, n. 6, p. 695

By:

SHAH, ANUJA R.;
GOYAL, R. K.

Publication type:

Article

EMPIRICALLY ASSESSING 510(K) DEVICE SAFETY.

Published in:

Jurimetrics: The Journal of Law, Science & Technology, 2023, v. 63, n. 2, p. 113

By:

Horvath, George

Publication type:

Article

Reversible EOL-Indicator: A New Cause for Low Pacemaker Rate.

Published in:

Pacing & Clinical Electrophysiology, 1983, v. 6, n. 3, p. 680, doi. 10.1111/j.1540-8159.1983.tb05325.x

By:

Scheibelhofer, W.;
Kaliman, J.;
Laczkovics, A.;
Mayr, H.;
Weber, H.;
Kaindl, F.

Publication type:

Article

Clinical Investigation of New Implantable Pacemakers.

Published in:

1983

By:

Furman, Seymour

Publication type:

Editorial

Act to keep patients safe: Device-related adverse event reporting

Published in:

Otolaryngology-Head & Neck Surgery, 2010, v. 142, n. 5, p. 651, doi. 10.1016/j.otohns.2009.10.017

By:

Schoem, Scott R.;
Shah, Udayan K.

Publication type:

Article

The dangers of the fast track.

Published in:: 2011
Publication type:: Editorial

BayesWeb: A User-Friendly Platform for Exploratory Bayesian Analysis of Safety Signals from Small Clinical Trials.

Published in:

Journal of Biopharmaceutical Statistics, 2011, v. 21, n. 5, p. 1030, doi. 10.1080/10543406.2011.590924

By:

Scott, JohnA.;
Hand, AustinL.;
Sian, LaylaS.

Publication type:

Article

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:

Bonangelino, Pablo;
Irony, Telba;
Liang, Shengde;
Li, Xuefeng;
Mukhi, Vandana;
Ruan, Shiling;
Xu, Yunling;
Yang, Xiting;
Wang, Chenguang

Publication type:

Article

How safe are new medical devices?

Published in:

Research Ethics, 2012, v. 8, n. 1, p. 43, doi. 10.1177/1747016112440391

By:

Humphreys, Stephen J.

Publication type:

Article

Publications Update.

Published in:: Journal of Medical Engineering & Technology, 2015, v. 39, n. 1, p. 89, doi. 10.3109/03091902.2015.995908
Publication type:: Article

Publications Update.

Published in:: Journal of Medical Engineering & Technology, 2012, v. 36, n. 6, p. 328, doi. 10.3109/03091902.2012.707474
Publication type:: Article