We use cookies to provide you with a better experience. By continuing to browse the site you are agreeing to our use of cookies in accordance with our Cookie Policy.
The International Electronics Manufacturing Initiative (iNEMI) has started a "Medical Components Reliability Specifications Project" to develop testing and use condition guidelines for electronic components and circuit boards used in medical devices.
Devicemakers need to design products that will work in the high-tech hospital environment of the future, experts said at a conference last month. Read More
Standards are mature enough now for businesses to embrace electronic data capture (EDC) and feel the positive impact almost immediately, Fast Track CEO Ed Seguine told PIR.
The global market for radio-frequency identification (RFID) tags will surge to $2.1 billion by 2016 from $90 million this year, says a new survey by IDTechEx.
Electronic data capture (EDC) proponents may have oversold the technology as a “panacea” to cure all etrial operational challenges, but the reality of user difficulties and technology aversion has slowed EDC adoption, experts told PIR.
Electronic data capture (EDC) is temporarily on the downward arc of a predictable acceptance rollercoaster ride, EDC advocate and Nextrials CEO James Rogers told PIR.
Clinical trials sponsors considering a potential clinical site can gauge whether a site has a strong edata compliance programit by how well it documents training and standard operating procedures (SOPs), said an industry expert.
The FDA last week initiated a pilot project to test a Health Level 7 (HL7) data interchange standard for submitting product stability data
to the agency.
The key to successful conversion from paper clinical trial records to electronic data capture (EDC) is in the advance preparation, said a key figure at Procter & Gamble (P&G).