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2014-08-31 23:03:49

Datex Pharmaceutical Software now includes a suite of features which enables compliance of the new FDA regulation, the Drug Quality Security Act (DQSA). Clearwater FL (PRWEB) August 31, 2014 Datex Pharmaceutical Software now includes a suite of features which enables compliance of the new FDA regulation, the Drug Quality Security Act (DQSA). The FDA Drug Quality and Security Act (DQSA) was signed into law in late 2013. Established to address threats to patient safety and security, the...

2014-08-26 23:17:21

VEEDIMS receives certification for demonstrating its ability to consistently provide product or service to meet customer and legal requirements, enhancing customer satisfaction and opening the way to continual improvement. VEEDIMS also meets requirements specific to the aerospace industry. Fort Lauderdale, Florida (PRWEB) August 26, 2014 VEEDIMS, LLC, a provider of “smart” integrated power and data Internet of Things (IoT) technology solutions to improve monitoring and control,...

2014-08-26 12:32:37

FALLS CHURCH, Va., Aug. 26, 2014 /PRNewswire-USNewswire/ -- Acentia, a premier provider of technology and management solutions, today announced that it has been appraised at the Carnegie Mellon University CMMI Institute's Capability Maturity Model Integration (CMMI) Level 4 for Development for its software development and maintenance work, bringing the entire company up to this process maturity benchmark. CMMI is a process improvement approach that provides organizations with the...

2014-08-21 23:15:46

Nel-Tech Labs, Inc. completes its ISO 9001:2008 recertification audit. Derry, NH (PRWEB) August 21, 2014 Nel-Tech Labs, Inc. is proud to announce it is has successfully completed its ISO 9001:2008 recertification audit. Nel-Tech Labs received its original ISO 9001:2008 certificate of registration on September 23, 2011 and this new recertification will bring us to the year 2017. To maintain our 3-year certification, NQA USA (an independent ISO registrar) performs yearly audits to ensure...

2014-08-21 23:14:15

In four hours, John Avellanet delivers proven, practical techniques for fast, flexible, flawless inspectional handling and response. Attendees will leave the session with a complete inspection SOP and an observation closure matrix, able to prove to an investigator they’re in a “state-of-control” and, if the worst happens, go from 483 observation to a coveted Untitled Letter without ever triggering a Warning Letter. Falls Church, VA (PRWEB) August 21, 2014 Flawless FDA Inspection...

2014-08-20 23:12:13

The Virginia Forum for Excellence is the premier event for performance improvement professionals in Virginia and the District of Columbia to network and learn about the nation’s Baldrige Criteria for Performance Excellence. Richmond, VA (PRWEB) August 20, 2014 The 32nd annual Virginia Forum for Excellence, sponsored by the non-profit United States Senate Productivity and Quality Award for Virginia (Virginia SPQA) is Virginia and District of Columbia's premier event focused on...

2014-08-20 08:20:56

Achievement Highlights Continuous Commitment to Quality, Process Improvement and Effective Delivery of System and Software Engineering Services FAIRFAX, Va., Aug. 20, 2014 /PRNewswire/ -- Salient Federal Solutions, Inc. (Salient), a leading provider of information technology, training, engineering, and intelligence analytic services to agencies in the intelligence, defense, homeland security, cyber security, and federal civilian markets today announced that it has been appraised at...

2014-08-19 23:09:25

NT Concepts announces its successful appraisal at Level 2 of the CMMI Institute’s Capability Maturity Model Integration (CMMI) for Services (CMMI-SVC). Vienna, VA (PRWEB) August 19, 2014 The appraisal, performed by The Process Company, LLC (TPC), concludes the second phase in NT Concepts’ pursuit of CMMI maturity. NT Concepts plans to achieve Level 3 for services and development by late 2014. CMMI is a process improvement approach proven to advance organizational performance. An...

2014-08-18 23:01:11

Device manufacturers understand that they must answer the two key design verification and validation questions: did they make the product right and did they make the right product? Learn proven tactics and tools to develop a strong statistical methods program — and a thorough understanding of what FDA auditors look for when they come for an inspection. Falls Church, VA (PRWEB) August 18, 2014 Choosing the Best Device Sample Size for Verification and Validation: Tools to Safely Speed...

2014-08-14 23:11:14

With 15 interactive exercises, this workshop, taught by internationally renowned medical device process validation expert Dan O’Leary, is designed to provide industry best practices to achieve sustainable process validation with regulatory bodies around the world. Attendees will learn the theories of process validation and documentation and how to put them into practice. Falls Church, VA (PRWEB) August 14, 2014 Innovative Process Validation Strategies for Medical Devices: Proving Your...


Word of the Day
vermicular
  • Like a worm in form or movement; vermiform; tortuous or sinuous; also, writhing or wriggling.
  • Like the track or trace of a worm; appearing as if worm-eaten; vermiculate.
  • Marked with fine, close-set, wavy or tortuous lines of color; vermiculated.
  • A form of rusticated masonry which is so wrought as to appear thickly indented with worm-tracks.
This word ultimately comes from the Latin 'vermis,' worm.
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