Date(s) And Time(s):
Mar 30 2012 8:00AM - Mar 30 2012 5:00PM

Location:
DIA
800 Enterprise Rd Ste 200,
Horsham, PA 19044-3509

http://www.diahome.org/DIAHome/Education/FindEducationalOffering.aspx?pr... Course

Overview:

Gain the basic knowledge required to conduct clinical trials, including information about subject safety, regulations, and the practicalities of performing research studies.

What You Will Learn

· Roles and responsibilities of each member of the study team

· Regulations and guidelines that govern clinical investigations

· Informed consent elements and processes

· Successful patient recruitment and retention strategies

· Adverse event handling and reporting

· Preparing for audits and audit process

Unless otherwise disclosed, the statements made by speakers represent their own opinions and not necessarily those of the organization they represent, or that of the Drug Information Association. Speakers, agenda and CE information are subject to change without notice. Recording of any DIA educational material in any type of media is prohibited without prior written consent from DIA.

Learning Objectives:

At the conclusion of this activity, participants should be able to:

· Identify the roles and responsibilities of each member of the study team including the clinical investigator, sub-investigator, study staff, IRB, and sponsor

· Apply the regulations and guidelines for conducting safe and effective clinical trials

· Describe the various processes for informed consent

· Recognize successful patient recruitment and retention strategies

· Understand requirements reporting adverse events

Target Audience:

· Clinical investigators

· Clinical research professionals

· Sub-investigators

· Study staff

Event Code:
12412

Contact Information:

For registration questions, please contact Vicki Adkinson at (215) 4426162 or Vicki.Adkinson@diahome.org
For agenda details, please contact Colleen Buckley at (215) 442-6108 or Colleen.Buckley@diahome.org