he Research Compliance Conference you cannot miss if you work for a sponsor, a research site, or for clinicians who conduct research Learn about updates to the new CMS Clinical Research Policy (replacing the Medicare NCD for Clinical Trials), latest trends on compliance with research accounting standards, clinical trial billing and process improvement, effort reporting, scientific misconduct, conflicts of interest, off-label use issues, FDA compliance, and government enforcement trends. Hear directly from representatives from NIH, OHRP, ORI, the FDA, the OIG, and the DOJ, and from other industry experts who can provide practical perspectives for handling research compliance risks.
   
 

Research Compliance Conference
June 3-6, 2012 in Austin, TX

Register Online | Brochure with fax registration | Exhibitor & Sponsor Prospectus

Come to Austin, TX June 3 – 6, 2012 to learn best practices and the latest thinking on:

  • New Rules for IRBs – What the (A)NPRM Could Mean for Your Institution
  • Increased Scrutiny on Pharmaceutical and Medical Device R&D Activities – The Impact on Clinical Research Sites
  • Clinical Research Enforcement Initiatives and False Claims Act Update
  • Successful FDA Inspections: How to Prevent and Respond to Common FDA Observations in a Form 483 or Warning Letter
  • Recent Developments in Clinical Trial Regulation and Oversight

Register today and enjoy the flexibility of two conferences for the price of one!

*Registration includes complimentary access to SCCE’s Higher Education Compliance Conference

Complimentary access to SCCE's Higher Education Compliance Conference is included with your Research Compliance Conference registration. The parallel schedule gives you the freedom to attend sessions at either conference—two for the price of one.


Can’t Join Us In June? Come to a Research Academy — Get The Latest Information — Get Certified

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