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Articles 1-21 out of 21 article(s) Title Author Type Date Words Premier Healthcare Alliance Endorses Supply Chain Standards to Enhance Patient Safety, Reduce Costs. Jul 21, 2008 652 Comparative effectiveness institute to be proposed. Apr 8, 2008 729 Building good fences: standards writers lay the foundations for risk management. Miller, Marc Mar 1, 2008 1815 New Report 'Standard and Specialty Medical Beds Therapeutic Surfaces Worldwide' Provides Detailed Market Estimates and Forecasts in U.S. Dollars. Industry overview Jan 28, 2008 555 Compliance With FDA And SEC Disclosure Requirements For Medical Device Makers: Standard Operating Procedures Can Help. Gray, Elizabeth Jan 23, 2008 617 Cave paintings, Black Swans and standards: practitioners' perspectives on risk management. Miller, Marc Jan 1, 2008 1193 Xlear, Inc., Orem, UT, has achieved ISO 9001:2000 and ISO 13485:2003 certification for quality management, which is the recognized international standard for medical device regulations around the world. Nov 1, 2007 86 Newly Launched B. Braun Contiplex(R) Stim System Redefines Standards for Stimulating Catheters. Oct 14, 2007 441 National Standards Authority of Ireland Redefines the Medical Device Approval Process. Jul 23, 2007 373 Adept Technology Selected by Integrated BioSciences, Inc. as Robotics Partner for Standard Medical Platform. Mar 20, 2007 494 What are your standards? van de Zande, Rene Mar 1, 2007 1363 CDRH not dividing pre-/post-market adverse reports; AEs and recalls increasing. Pickett, Joseph Feb 12, 2007 926 Medidata Solutions Leads Global Education on Clinical Data Management, Standards and Safety at DIA Industry Events. Oct 4, 2006 614 dj Orthopedics to Offer Soccer Headgear in Response to New ASTM Sports Safety Equipment Standard. Apr 19, 2006 696 Preparing for CMS's continence care revisions: how to get a head start on the new requirements in this key area. Underwood, Reta A. May 1, 2005 749 EndoMed hit with no FDA-approved IDE, no PMA. Gould, Dawn Brief Article Jul 1, 2003 153 FDA hits ventilatory recorder manufacturer with failure to establish design control procedures. Gould, Dawn Jun 1, 2003 511 Device validation should be 'stable and capable,' FDAer says. Huegel, Kelly Brief Article Dec 1, 2001 621 EUROPEAN DIRECTIVE ON MEDICAL TESTING DEMANDS TRACEABILITY. Brief Article Mar 1, 2001 206 FDAer touts finding impurities at 1/10th of percent in batches. Brief Article Aug 1, 2000 263 Battle rages over managed care reform; device manufacturers lag in Y2K compliance. Szabo, Joan Sep 1, 1998 678