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Understanding Costs of a Study for Clinical Trials

 
  May 22, 2012  
     
 
ComplianceOnline, Online Webinar
2012-06-15


Why Should You Attend:

Determining an appropriate clinical trial budget to ensure a study can be completed is challenging for both sites and sponsors. Whether you are new to clinical research, or have years of experience, there are 3 areas of expertise you may not have mastered - understanding and outlining costs, negotiating budgets, and complying with criteria (Medicare provisions for determining Qualifying Trials and Routine Care). If not, you may be a site that is underwriting sponsors costs, or you may be a sponsor that is overpaying site costs, and both sites and sponsors may be incorrectly submitting non-qualifying costs to insurers.

Learning Objectives:

At the end of this webinar, participants will understand categories of study costs and be able to identity costs that sponsors are expected to cover.

Areas Covered in the Seminar:

  • Start-Up Costs.
  • Fixed Costs.
  • Variable Costs.
  • Hidden Costs.
  • Overhead.
  • Qualifying Trials and Routine Care.
  • Developing a Cost Plan.
  • Negotiating a Budget.

 

 
 
Organized by: ComplianceOnline
Invited Speakers: Jennifer Holcomb, MA, CCRC, is a clinical research professional with 20 years of experience in the field. Currently employed by Duke University, she provides guidance and leadership in the establishment and development of policies in the conduct and management of clinical research. Key areas of expertise include clinical trial budgeting and contract negotiations as well as regulatory knowledge including international ICH GCP standards. Jennifer has extensive experience in training and education and serves as Vice Chair of the ACRP Professional Development Committee
 
Deadline for Abstracts: 2012-06-15
 
Registration:

For Registartion:

 http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=702332?channel=hummolgen

E-mail: referral@complianceonline.com
 
   
 
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