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Pharmaceutical Executive
November 1, 2006
Unraveling the eSource Industry-wide standards for electronic patient data have long felt like buried treasure. Companies today are getting closer - by way of a tangled map. mark for My Articles similar articles
Bio-IT World
Dec 2005/Jan 2006
Mark D. Uehling
Convergence of EHR and EDC The hypothesized convergence of applications and databases for drug development, clinical trials, hospitals, and physicians is both closer and more distant. mark for My Articles similar articles
Bio-IT World
March 10, 2003
Spink & Blumenstiel
Getting IT Right Applying information technology to trials can boost productivity. Here's a strategic framework for going e-clinical. mark for My Articles similar articles
InternetNews
August 25, 2010
Security, EMRs Top Healthcare IT Priorities With new government regulations placing even more responsibility and scrutiny on the healthcare industry, IT administrators are struggling to deliver both efficiency and security. mark for My Articles similar articles
Bio-IT World
March 10, 2003
Kenneth Getz
E-Clinical Technology Overview Clinical trial researchers want to leverage the benefits of IT -- and now they can for every core process. But they also have to get past the barriers to adoption. mark for My Articles similar articles
Bio-IT World
May 9, 2003
Mark D. Uehling
Data Rapture? Electronic capture of data: Some say it unclogs the medieval clinical trials process. Others remain skeptical of software and put their trust in paper. mark for My Articles similar articles
Bio-IT World
November 14, 2003
Amnon Shabo
Integrated EHR: The Final Frontier Harmonizing various standards for electronic health records will have far-reaching effects on bioinformatics. mark for My Articles similar articles
CIO
September 23, 2010
Neil Versel
Healthcare IT: How Reform Is Giving CIOs A More Strategic Role in Delivering Patient Care Electronic health records aren't enough. Healthcare CIOs need to apply technology to coordinating patient care and measuring quality. mark for My Articles similar articles
Bio-IT World
March 17, 2004
Speeding EDC Adoption Implementation by clinical sites is lumbering along at an unimpressive rate. Here's what must be done to speed things up mark for My Articles similar articles
Bio-IT World
February 2007
Beth Harper
Meshing EDC with CTMS Many unsolved problems in conducting clinical trials cause delays, wasted resources, team frustration, and even safety issues. Thus, the industry is turning more of its attention away from Electronic Data Capture to Clinical Trial Management Systems. mark for My Articles similar articles
Bio-IT World
July 2005
Mark D. Uehling
'E-source' Is Coming, Experts Say The odd marriages of the ancient and modern in clinical technologies were in evidence at the E-Clinical Trials & Research conference program. There was evidence of the adoption of advanced and robust commercial software -- even toward clinical trials that do not use paper, though most do. mark for My Articles similar articles
HBS Working Knowledge
March 26, 2014
Dina Gerdeman
How Electronic Patient Records Can Slow Doctor Productivity Electronic health records are sweeping through the medical field, but some doctors report a disturbing side effect. Instead of becoming more efficient, some practices are becoming less so. Robert Huckman's research explains why. mark for My Articles similar articles
Bio-IT World
March 17, 2004
Strategic Insights Clinical Trials Major drug developers have put electronic data capture to the test and found benefits ranging from instant data access to fewer truckloads of paper. Yet many clinical sites are slow to accept the technology. mark for My Articles similar articles
Bio-IT World
March 17, 2004
Kenneth Getz
Getting Past No Low adoption rates of e-clinical trial technology can't be blamed on external market dynamics alone. Biopharmas must face four inhibitors within their own organizations mark for My Articles similar articles
Bio-IT World
July 2005
David Fishbach
Does EDC Herald the End of CTMS? Clinical trial managements systems (CTMSs) and Electronic data capture systems (EDCs) are compared with respect to their history, advantages and disadvantages. Studies suggest both have enough advantages to survive in some form of integrated solution. mark for My Articles similar articles
Bio-IT World
April 15, 2003
Paul Bleicher
E-Sourcing: Covering the Regulatory Bases Capturing clinical source data electronically can hit a home run for trial efficiency and safety -- but access control is key. Here's an expert guide. mark for My Articles similar articles
Nursing Management
September 2010
Richard Hader
The evidence that isn't... Interpreting research When patients seek a healthcare practitioner for services, they believe that the delivered care is based on proven science. But reality is far from patient perception. In fact, most care is still based on anecdote, not evidence. mark for My Articles similar articles
Insurance & Technology
August 9, 2010
Nathan Golia
Humana, Athenahealth Partner to Spur EHR Adoption The health insurer joins a growing list of peers providing financial or other incentives to providers to adopt electronic health records. mark for My Articles similar articles
Pharmaceutical Executive
September 1, 2013
Ben Comer
Share of Screen: Prioritizing Electronic Health Records Are electronic health records a viable channel for engagement? mark for My Articles similar articles
Bio-IT World
May 2006
Mark D. Uehling
Clinical Speakers Enjoy Industry Acceptance For the first time at the Bio-IT World Conference, the clinical speakers did not wring their hands about whether their tools would be accepted by the industry. This year, it was a question of how quickly technology would be used to expedite trials and raise the quality of the data therein. mark for My Articles similar articles
Insurance & Technology
August 4, 2009
John Reynolds
Electronic Health Records: A Place to Start, Not a Destination End-game electronic health record solutions need to focus on integrating individuals' health with wealth and making it personal and actionable in a consumer-directed healthcare world. mark for My Articles similar articles
Pharmaceutical Executive
August 1, 2011
Ben Comer
An IOU to Big Pharma Regarding EHR It's a work in progress among electronic health records providers to offer a clear bridge between pharma and physicians. mark for My Articles similar articles
Bio-IT World
November 2006
Mark D. Uehling
Putting EDC on the Fast Track There's no escaping the imposing numbers of choices in launching a clinical trial using electronic data capture. Is there a better way? Clinical trial consultant Fast Track Systems says it has one. mark for My Articles similar articles
Bio-IT World
May 2006
Nick Richards
The Unifying Power of Ajax Asynchronous JavaScript and XML (Ajax) will simplify the collecting of clinical trials data. As the pharmaceutical industry and contract research organizations moves toward electronic data capture, Ajax technology can smooth the way. mark for My Articles similar articles
Bio-IT World
January 21, 2005
How IT Can Decrease Time-to-Market in Clinical Trials Pharma manufacturers can learn from their industrial counterparts: Integrating systems can accelerate product delivery. mark for My Articles similar articles
Pharmaceutical Executive
July 1, 2006
Jeannette Park
Roundtable: Are We There Yet? How About Now? Now? Can Electronic Data Capture become the industry standard for clinical trials? In this roundtable discussion, six early adopters reveal where they struggled, and what you need to know to implement this new technology. mark for My Articles similar articles
Bio-IT World
May 19, 2004
Mark Uehling
Patients Without Borders As biotech companies search for patients abroad, technology clearly matters--but not every clinical trial on the planet is ready for electronic data capture. mark for My Articles similar articles
Bio-IT World
February 2006
Chris Connor
Has EDC Jumped the Shark? As data management teams begin to deploy electronic data capture in their clinical trials, "cool" gives way to the cool reality that IT investments have to produce real results. mark for My Articles similar articles
Nursing Management
October 2011
Edna Cadmus
Your role in redesigning healthcare We need to rethink how we provide care and to understand the interconnectedness and the structure of healthcare by looking at it as a whole vs. the sum of its parts. As leaders we need to view the evidence as we rethink healthcare together. mark for My Articles similar articles
Bio-IT World
April 16, 2004
Joel Hoffman
Taking the Trial Out of Clinical Outsourcing Make sure the vendor's standard operating procedures will mesh with your own, and then tirelessly work toward systems integration. mark for My Articles similar articles
CRM
June 2012
Leonard Klie
Modern Medicine: A Marketing Headache When it comes to customer self-service, the medical industry is far ahead of many other verticals in its use of technology, but customer use of those options is still far from prevalent. mark for My Articles similar articles
Bio-IT World
August 2005
Ellen H. Julian
Tech Expertise Singles Out Outsourcers Biopharmaceutical companies are flocking to consultants, outsourcers, and staffing firms to help with discrete clinical trial processes to gain access to advanced technologies and reduce the drain on already-scarce IT resources. mark for My Articles similar articles
Pharmaceutical Executive
November 1, 2012
Sue Barrowcliffe
Real World Insights Commercial teams as well as patients can benefit from managed access programs, which are designed to provide access to medicines outside of the clinical and commercial setting, for patients who have no other available treatment options. mark for My Articles similar articles
Pharmaceutical Executive
September 1, 2008
Melanie North
Publish or Perish FDAAA means that companies need to register clinical trials; and not only for publication planning. mark for My Articles similar articles
Pharmaceutical Executive
March 1, 2014
Jill Wechsler
Data disclosure, integrity challenge pharma Transparency initiatives are multiplying, affecting research, marketing and compliance. mark for My Articles similar articles
Bio-IT World
June 2006
Mark D. Uehling
Afferenz on EDC, Images, and Data Integration There are people who think the outsourcing of IT to India will not affect the life sciences. But companies like Afferenz raises concerns about U.S. companies lagging behind Indian companies on laying the foundation for clinical trials. mark for My Articles similar articles
CIO
August 27, 2013
Brian Eastwood
Healthcare IT Struggles to Keep Up With Mobile Health Demands While healthcare struggles with unique legal and regulatory impediments that other fields don't face, it's also poised to gain much more from what some call a 'mobile revolution.' mark for My Articles similar articles
Bio-IT World
March 17, 2004
Paul Bleicher
Winning at EDC Implementation Adoption may be lagging at the enterprise level, but there's a stalwart group of biopharmas making EDC happen. Here's how they're doing it mark for My Articles similar articles
Bio-IT World
January 13, 2003
Mark D. Uehling
Powerhouse CRO (Slowly) Goes Electronic Unhappy customers at Quintiles -- the world's largest CRO (contract research organization) -- are rare. It kept plugging away at the startup process, redesigning it from scratch. Now starting electronic trials takes no longer than paper ones. mark for My Articles similar articles
Pharmaceutical Executive
July 1, 2005
Rob Case
In Search of the Holy Grail Chasing ultimate clinical trial efficiency, one small step at a time. A carefully considered approach to data integration can benefit every stakeholder from the investigator to the pharmaceutical executive. mark for My Articles similar articles
Bio-IT World
August 18, 2004
Mark D. Uehling
Master of the EDC Universe An interview with Sylva Collins, global head of advanced clinical systems at Novartis, who in the case of electronic data capture (EDC), proved to the pharmaceutical industry that technology could be transformative in clinical trials. mark for My Articles similar articles
Bio-IT World
June 2005
Mark D. Uehling
Abandon Paper! Use a PDA! The entire pharmaceutical industry is migrating away from paper diaries, fraught as they are with patients' well-meaning but well-documented procrastinations and fabrications. But electronic gadgets are not inexpensive, even for rich sponsors of clinical trials. mark for My Articles similar articles
Nursing Management
December 2011
Brenda Kulhanek
EMR development...Always be prepared Implementing an electronic medical record system offers countless benefits: major healthcare savings, reduced medical errors, improved quality of healthcare, and improved health. mark for My Articles similar articles
CIO
May 31, 2011
Fred O'Connor
Hospitals Compete for IT Talent with Funding At Stake Health care providers in the U.S. are encountering a lack of qualified candidates as they race to meet federal government deadlines for electronic health record and health IT use. mark for My Articles similar articles
Insurance & Technology
August 18, 2010
Nathan Golia
Insurers Take Lead in EHR Implementation With guidelines for meaningful use of electronic health records established, health carriers expect IT improvements on the provider side to lower healthcare costs by reducing care redundancies and readmissions. mark for My Articles similar articles
Pharmaceutical Executive
June 1, 2007
Dinh Nguyen
Clinical Trials Under Scrutiny Over the last few years, there has been a growing number of instances of misconduct in clinical research. mark for My Articles similar articles
Pharmaceutical Executive
January 1, 2011
Singh & Glozman
Managing Clinical Trials in Emerging Markets Amgen's hub-and-spoke system combines control at home with the flexibility to respond to local needs. mark for My Articles similar articles
Bio-IT World
April 16, 2004
Mark Uehling
PDAs and Clinical Trials PalmOne's director of healthcare sales explains why clinical trials are driving sales of handheld devices. mark for My Articles similar articles
Bio-IT World
August 13, 2002
Mark D. Uehling
Clinical Trial Data Management: Tortured by Paper Reams of paper stuffed into boxes and shipped to the FDA by the truckload is hardly the best approach to drug approval. But what's the right way? mark for My Articles similar articles
Pharmaceutical Executive
March 1, 2013
Ken Getz
Building Clinical Trial Awareness for Patients: Why Not Try the Pharmacist? The author explains how building a stakeholder outreach agenda around the community pharmacist can lead to a better outcome in managing the complex ins and outs of a trial protocol. mark for My Articles similar articles