Greenlight Guru Acquires Electronic Data Capture Solution SMART-TRIAL
(Greenlight Guru: Indianapolis, IN)--Greenlight Guru, pioneer of the Medtech Lifecycle Excellence Platform, has acquired SMART-TRIAL, maker of
Exemplar Global and QLBS Partner to Launch Audit Simulator
(Exemplar Global: Milwaukee) -- Just like aviation flight simulators, the Audit Simulator provides opportunities to audit without risk.
New Device Can Diagnose Covid-19 From Saliva Samples
First published Aug. 6, 2021, on MIT News.
NIST Prize Challenge Launches Research for Unmanned Aircraft in Search and Rescue
(NIST: Boulder, CO)— The U.S. Department of Commerce’s National Institute of Standards and Technology (NIST) has launched a new prize competition to advance the use of unmanned aircraft systems (UAS) in first responder search and rescue operations.
Greenlight Guru Launches Greenlight Guru Academy
(Greenlight Guru: Indianapolis) -- Greenlight Guru, the leading medical device quality management software (MDQMS) platform, announces the launch of
Streamlined Salmonella Testing Drives Efficiencies, Enables Flexibility, Solves Problems
(Thermo Fisher Scientific: Basingstoke, UK) -- A quick and easy culture-based method for the enrichment, detection, and confirmation of Salmonella species has been validated for the broadest range of food, animal feed, and environmental samples, and is
Chip on a Card Would Detect Covid-19 Antibodies in a Minute
(University of Rochester: Rochester, NY) -- Researchers in Rochester are developing an optical chip on a disposable card that can detect exposure to multiple viruses within a minute—including the coronavirus that causes Covid-19—from a single drop of blood.
First -80°C Liquid Nitrogen-Based, Automated Storage System to Offer Inventory Control, Reporting Capabilities
(Brooks Life Sciences: Chelmsford MA) -- Brooks Life Sciences, a division of Brooks Automation, announces the immediate availability of
International Standard for Medical Device Testing Updated
(ISO: Geneva) -- Clinical investigation of medical devices is naturally highly regulated, with numerous national and regional rules and requirements that must be adhered to by manufacturers and investigators, as well as other parties involved in clinical trials.