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Nursing Management November 2009 Kathleen Russell-Babin	Seeing through the clouds in evidence-based practice Evidence-based practice is analyzing the research available as critically as possible, placing the findings in the context of your organization, and adding the perspectives and judgment of clinicians and patients.
D-Lib Jan/Feb 2012 David Shotton	The Five Stars of Online Journal Articles -- a Framework for Article Evaluation I propose five factors -- peer review, open access, enriched content, available datasets and machine-readable metadata -- as the Five Stars of Online Journal Articles.
D-Lib Jul/Aug 2012 Bertin & Atanassova	Semantic Enrichment of Scientific Publications and Metadata Our aim is to bring new value to scientific publications by automatic extraction and semantic analysis.
D-Lib Sep/Oct 2014 Latif et al.	Exposing Data From an Open Access Repository for Economics As Linked Data This article describes an approach to publishing metadata on the Semantic Web from an Open Access repository to foster interoperability with distributed data.
Pharmaceutical Executive October 1, 2005 Lisa Grimes	Clear Road Ahead An industry standard for publicizing clinical-trial results is a ways off. But pharma's openness to more transparent procedures is moving things in the right direction.
D-Lib Jan/Feb 2015 Bontcheva et al.	Semantic Enrichment and Search: A Case Study on Environmental Science Literature In order to facilitate environmental science researchers in carrying out better semantic searches, a form-based semantic search interface is proposed.
D-Lib Nov/Dec 2010 Byrne & Goddard	The Strongest Link: Libraries and Linked Data This article will outline some of the benefits that linked data could have for libraries, will discuss some of the non-technical obstacles that we face in moving forward, and will finally offer suggestions for practical ways in which libraries can participate in the development of the semantic web.
Managed Care May 2000 Mark G. Weiner, M.D., and Eric Pifer, M.D.	Computerized Decision Support and the Quality of Care The notion of quality of care in medicine is not new, but it is becoming increasingly important as the competitive health care market demands objective measures to compare physicians, hospitals, and managed care organizations....
D-Lib Jul/Aug 2010 Powell et al.	Semantically Enhancing Collections of Library and Non-Library Content Many digital libraries have not made the transition to semantic digital libraries, and often with good reason.
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.
Bio-IT World April 2007 Eric K. Neumann	Building Biomedical Ontologies Ontologies take time and commitment to be constructed, but their value increases dramatically when they are well structured and logically consistent, especially across multiple domains. The success of the NCBO will have a direct effect on the success of biomedical research in all areas.
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.
D-Lib June 2006 Zeng & Chan	Metadata Interoperability and Standardization - A Study of Methodology Part II: Achieving Interoperability at the Record and Repository Levels Information professionals must give high priority to the task of creating and maintaining the highest feasible level of interoperability among extant and new information services.
D-Lib January 2006 Linden & Green	Don't Leave the Data in the Dark: Issues in Digitizing Print Statistical Publications Statistical digitization projects must make investments in adequate metadata and object-oriented design at the point of digitization - otherwise, the data are in danger of losing their context
Pharmaceutical Executive May 1, 2006 Madison, Chan & Seeger	Making the Link The FDA recognizes that a new drug standard must evolve -- one of routine, proactive safety surveillance. But post-marketing safety studies are too slow. Here's how pharmaceuticals are using claims databases to solve the problem.
Information Today December 14, 2009	Wiley-Blackwell Launches New Online Medical Reference Tool Synthesized from the most timely and late-breaking clinical evidence derived from the most respected medical authorities, this topic-oriented clinical resource tool is designed to help clinicians more effectively make diagnoses, chart treatment plans, and determine prognoses.
D-Lib Nov/Dec 2015 Herrmannova & Knoth	Semantometrics in Coauthorship Networks: Fulltext-based Approach for Analyzing Patterns of Research Collaboration We explore how Semantometrics can help to characterize the types of research collaboration in scholarly publication networks and the nature of the cross-community ties, and how this information can be utilized in aiding research evaluation.
D-Lib June 2002 Paul Shabajee	Primary Multimedia Objects and 'Educational Metadata' A fundamental dilemma for developers of multimedia archives.
Pharmaceutical Executive June 9, 2014 Getz et al.	Adaptive Trial Design: Prepping for Adoption Biopharmaceutical companies are targeting improvements in clinical trial design as a critical factor in pipeline portfolio success.
Reason October 2007 Ronald Bailey	Is Industry-Funded Science Killing You? The overrated risks and underrated benefits of pharmaceutical research "conflicts of interest."
D-Lib October 2009 Papadakis et al.	Subject-based Information Retrieval within Digital Libraries Employing LCSHs The goal of this article is to semantically exploit the explicit and implicit relations between Library of Congress Subject Headings in order to provide more effective subject-based, information retrieval within digital libraries.
Bio-IT World November 14, 2003 Jeff Augen	Making Information-Based Medicine Work A confluence of scientific discovery and high-throughput technology has made information-based medicine possible -- and imperative.
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.
Bio-IT World October 2005 Salvatore Salamone	Masters of the Semantic Web The Semantic Web is just at its early stage of deployment. As with the original Web, the usefulness of a Semantic Web will grow as more data and sites support RDF and the other Semantic Web standards.
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.
American Journal of Nursing November 2007	The NFP Model: The Evidence of the Evidence A lack of standardization among home visitation programs hinders an evaluation of the success of a program.
Bio-IT World July 11, 2002 Stephen T.C. Wong	Neuro-IT Needs Integrated Infrastructure There are two major motivations for merging enterprise solutions into clinical neuroscience. The first is the need to scale up the capacity for data management. The second is the economic benefits of data sharing, software reuse, and infrastructure build-out while reducing costs.
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.
D-Lib January 2004	In Brief LEADERS Toolkit Breaks New Ground... INSA e-Journals Project... CO-ODE - A Collaborative Open Ontology Development Environment... etc.
ONLINE Sep/Oct 2010 BeDell & Trudell	Does Taxonomy Matter in a New World of Search and Discovery In a Google world, even information professionals wonder if the traditional library information sources' reliance on controlled vocabularies remains a viable, worthwhile, and cost-effective strategy.
Pharmaceutical Executive November 1, 2014	EMA -- a Pioneer Permanently At Bay Agency's plan for reporting clinical trial data has sparked strong reactions from health campaigners, industry, and patients.
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.
Information Today February 16, 2004 Frank Cervone	W3C Delivers Standards for the "Semantic Web" With the recent announcement of two key recommendations by the World Wide Web Consortium, the "Semantic Web" has finally come of age.
Pharmaceutical Executive July 1, 2006 Derek Lowe	What You Need to Know About Adaptive Trials A handful of new statistical techniques and clinical-trial designs will let you change the way you run your business. Here's your guide to the basics.
Managed Care July 2005 Martin Sipkoff	Support Grows for Establishing National Clinical Trial Registry Stakeholders are pushing for a national clinical trial registry, and efforts by UnitedHealth Group are in the forefront. Medical journals are setting hard and fast rules.
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.
Pharmaceutical Executive April 1, 2007	Thoughtleader: Melissa Brown, Center for Value-Based Medicine Here, co-author Melissa Brown discusses her book Evidence-Based to Value-Based Medicine and what's driving the move toward value-based medicine, how it will affect pharma, and why executives should embrace it.
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.
Managed Care September 2005 Arthur Lazarus	Individual Wariness Needed To Spot Biased Drug Research Full and accurate disclosure of conflicts by researchers does not ensure the prevention of publication of articles that are misleading or otherwise biased. Impossible-to-enforce mandates won't work. Pharmacy directors and others must pose the right questions to the right people.
Bio-IT World October 10, 2003 Robert M. Frederickson	Capturing Clinical Information Ardais is building a repository of clinical samples and related patient data.
Chemistry World August 7, 2013 Emma Stoye	AllTrials releases plan for clinical trial reporting The organizations behind AllTrials, a public campaign calling for detailed information on clinical trials to be publically available, have put together a detailed plan on how to achieve clinical trial reporting on a global scale.
Managed Care June 2001 Darcy Lewis	National Guideline Clearinghouse: Extensive Resource Underused It's there on the Web, highly convenient. What keeps physicians away?
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?
Bio-IT World June 2006 Kevin Davies	The Data Deluge: Deal or No Deal? Far from decrying the data glut, researchers should embrace the complexity of genomic and other sources of data, particularly for its predictive properties in the field of personalized medicine.
Chemistry World July 31, 2013 Daniel Johnson	Animal testing failures put drug trial volunteers in danger The reporting of animal studies is biased, inflating the efficacy of drug candidates and pushing them into the clinic before they are ready.
American Family Physician June 15, 2004 Ramzi & Leeper	DVT and Pulmonary Embolism: Part I. Diagnosis The incidence of venous thromboembolic diseases is increasing as the U.S. population ages. Evidence-based algorithms help guide the diagnosis of these diseases.
Bio-IT World March 8, 2005 Mark D. Uehling	Is That a Target on Her Back? Q&A with Deborah Zarin, head of ClinicalTrials.gov, the matchmaking Web site for patients seeking to participate in federally sponsored clinical trials.
Pharmaceutical Executive June 1, 2005 Joanna Breitstein	Turn the Page Changes in ethics and expectations are driving the way pharma interacts with medical publishers.
D-Lib Jul/Aug 2012 Knoth et al.	Special Issue on Mining Scientific Publications Digital libraries that store scientific publications are becoming increasingly important in research. They are used not only for traditional tasks such as finding and storing research outputs, but also as sources for discovering new research trends.
Information Today May 13, 2013 Marydee Ojala	Cochrane's New Look At this year's Medical Libraries Association annual conference, held May 3-7, 2013, in Boston, several sessions centered on new and forthcoming developments with The Cochrane Collaboration.