February 10, 2012
| Digital Healthcare > Regulatory Policy


Regulatory Policy


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Health Care & Health-IT Under Obama Digital HealthCare & Productivity | WASHINGTON—The election of Barack Obama as president and the solidification of the Democratic majority in Congress clearly will have an effect on the national health care agenda for 2009, but some of the reasons might not be so obvious.

Health IT Certification Moves Forward Digital HealthCare & Productivity | WASHINGTON—The American Medical Informatics Association (AMIA) is turning its attention to medical specialty boards in its bid for recognition of clinical informatics as a distinct medical subspecialty, following the approval of detailed plans for physician informatician training and competency.

Fed Report Calls on NIH to Blaze Personalized Medicine Trail Digital HealthCare & Productivity | It’s a busy time on the personalized medicine front. The recently-released federal government report, Priorities for Personalized Medicine, is gradually attracting attention. The state of Wisconsin last week jumped into the race to become a center for personalized medicine. And a group of technology providers has joined Scripps Translational Science Institute (STSI) to study to what extent people make behavioral changes when they are provided with genetic screening and information about their various risk factors.

Certifying PHRs Digital HealthCare & Productivity | The first set of certification criteria for personal health records (PHRs) products will focus more on privacy, security, and interoperability with other health-IT and less on specific functionality in an effort to foster innovation in a relatively new market segment, according to the Certification Commission for Healthcare Information Technology (CCHIT).

CCHIT Certifies EHRs and HIEs Digital HealthCare & Productivity | On Tuesday, CCHIT said that eight ambulatory electronic health records (EHR) products earned full certification under the new 2008 criteria for interoperability. Tomorrow, CCHIT will open the first-ever application period for certification of health information exchanges (HIE).

Warfarin Test: Who Should Pay for Personalized Medicine? Digital HealthCare & Productivity | Payers, physicians, and the pharmaceutical industry are closely watching CMS deliberations over whether or not to pay for a genetic-based test that provides guidance on Warfarin dosing. The FDA, which approved the test, says it’s an important tool, but the CMS isn’t so sure and opened a National Coverage Analysis (NCA) on the subject in August.

Privacy Certification Program Aims to Ensure Patients’ Trust Digital HealthCare & Productivity | A former senior advisor in the Department of Health and Human Services (HHS) is heading up the first large-scale effort to certify health-IT products for adherence to privacy standards.

Lively Debate at HIPAA Summit at Harvard Digital HealthCare & Productivity | Are patient privacy rules effective? The answer is not a simple yes or no. “It’s working, but it’s got a ways to go,” suggests William Braithwaite, chief medical officer of San Diego-based security and identity management company Anakam.

Karen Trudel of CMS Talks about HIPAA Audits and NPI Issues Digital HealthCare & Productivity | In the wake of one of the largest fines levied by HHS for a HIPAA (Health Insurance Portability and Accountability Act) violation, HIPAA official Karen Trudel says to expect further audits and enforcement proceedings as federal officials begin to extend compliance reviews.

Security Features Not Limited to Paper Digital HealthCare & Productivity | Electronic prescribers who want to print prescriptions for Medicaid patients no longer will have to spend up to 10 times the cost of plain paper to comply with new tamper-resistance regulations, the result of intense negotiations between government officials, medical societies, the pharmacy industry, paper manufacturers, and two health-IT advocacy groups.

White Papers & Special Reports

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Managing the Modern Genomics Data Flood
Sponsored by SGI

Managing and storing the perfect storm of multi-disciplined data pouring from next generation sequencers and other omics instruments is a central challenge in life sciences. Discover in this paper how the SGI ArcFiniti storage solution, optimized for unstructured genomics and life sciences data can: 

  • Reduce costs, proactively protect data integrity, and deliver the high performance I/O required for genomics data processing and analysis.  
  • Effectively manage capacities from 156TB to 1.4PB as a disk based, integrated hardware and software platform 


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Turning Genomics Data into Practical Insight
Sponsored by SGI

With worldwide sequencing capacity approaching 13 quadrillion DNA bases annually turning genomics data into knowledge is a true computational challenge. Read this paper and learn how the SGI UV coherent shared memory platform can:  

  • Speed results time while cost competitively tackling the most difficult computational problems across all omics disciplines. 
  • Push performance by scaling to extraordinary levels, up to 256 sockets (2,560 cores, 4,096 threads) per single system (one OS image). 

Provide support for up to 16TB of coherent shared memory in a single system image enabling extreme efficiency across a wide range of compute demands. 



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New Complimentary Market Survey…
Collaborations and Communications Within Drug Discovery Research
Sponsored by Accelrys
This survey was conducted by the Cambridge Healthtech Media Group in January, 2012. It was sponsored by Accelrys related to their HEOS initiative to gather valid information around externalizing collaborative research while improving communications in the cloud. With 310 qualified industry respondents the survey findings reveal useful usage and trends patterns.  An insightful follow-on discussion and webinar related to this survey, and the HEOS by Scynexis SaaS portal is also available on the Bio-IT World website for complementary viewing.
 


Life Science Webcasts & Podcasts

medidata podcast #8 Meeting Today’s Challenges in Clinical Trial Supply Management
Sponsored by: Medidata Solutions Worldwide  

Setting up and managing the clinical trial involves many complex procedures. Among the most challenging are planning and executing the logistics of the trial’s clinical supplies. This podcast focuses in depth on the following topics which trace current practices and future evolution of this crucial aspect of clinical trials:

  • Current practices in clinical trial logistics
  • Comparing advances in clinical supply practices to  other aspects of clinical trials 
  • Where current practices fall short of meeting the challenges
  • Trends and evolving improvements that may change the way logistics are conducted

Listen Now  


More Podcasts

Job Openings

tessella logo 
Scientific Software Engineer
Boston MA
$70,000 to $95,000
 
Apply at http://jobs.tessella.com   

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Early Access Collaborations ManagersClick here to find out more and apply   

Oxford Nanopore's GridION technology, VP, Sales and Marketing Click to  Apply  



For reprints and/or copyright permission, please contact  Tim McLucas, (781) 972-1342, tmclucas@healthtech.com .