Region:  
 
      Advanced
Search 		 
Bookmark and Share 
  
Find An Educational Offering
Select Search Criteria
Keyword:
Events starting on or after:  mm/dd/yyyy
Events Added:
Region:
Interest Areas (IA): Hold the CTRL key to select or de-select multiple items from adjacent list box

     
Event Type: Hold the CTRL key to select or de-select multiple items from adjacent list box

 
 
© 2010 DIA  |  Home  |  Site Map  |  Contact Us  |  Terms and Conditions of Use  |  Disclaimer  |  Privacy Policy
  Click here to Expand the Tab 
10001 46th DIA Annual Meeting
 Overview 
 Agenda / Committee 
 Continuing Education 
 Tutorials / Sub-Events 
 Exhibits 
 Travel/Hotel Information 
 Registration Fees 
 Related Offerings 
 Highlights 
Title:
46th DIA Annual Meeting

Date(s) And Time(s):
Jun 13 2010 8:30AM - Jun 17 2010 12:30PM

Location:
Walter E. Washington Convention Center
801 Mount Vernon Place, NW
Washington, DC 20001-3614 

Interest Area(s):
CMC,Clinical Safety/Pharmacovigilance,Clinical Research,Clinical Data Management/ eClinical,Document Management/ eSubmissions,Quality Assurance/Quality Control,Medical Communications,Medical Writing,Nonclinical,Outsourcing,Project Management,Advertising & Promotion,Advertising & Promotion,Research & Development,Statistics

Overview:

Facilitating Innovation for Better Health Outcomes

The DIA Annual Meeting is the premier event for professionals involved in the discovery, development, and lifecycle management of  pharmaceuticals, medical devices, and related products. There is no other industry meeting of its kind that can rival the breadth and depth of experience that this meeting delivers. With 25 content-area tracks, 350 sessions and 20 tutorials, presentations are geared to attendees at all disciplines, works settings, and experience levels. The DIA Annual Meeting, above all others, offers valuable professional cross-functional learning and networking experiences.



Learning Objectives:

At the conclusion of this meeting, participants should be able to:
• Compare and contrast the current regional regulatory and public policy environment pertaining to pharmaceuticals and related products
• Discuss the regulatory and economic factors that impact the global biopharmaceutical industry
• Recognize the challenges facing regulatory agencies and industry in research study design and statistical methodology
• Assess the progress toward integrated, state-of-the-art document management systems
• Identify legal, advertising, and marketing issues related to providing product information
• Apply principles of risk assessment and management to development and postmarket phases of new healthcare products
• Summarize issues in safety reporting and data analysis regarding adverse events
• Distinguish regional approaches to integration of evidence-based medicine and comparative effectiveness research into healthcare decision-making
• Describe current issues in designing and implementing clinical trials, including patient recruitment, site selection and management of multiregional clinical trials
• Identify current opportunities and challenges in the area of personalized medicine for disease treatment



Target Audience:
This program is designed for individuals involved in the the discovery, development, and life cycle management of pharmaceuticals, medical devices, and related products. The program is intended to strengthen professionals' understanding of the value of cross-discipline integration and to foster innovation for better health outcomes.

Event Code:
10001

Contact Information:

Worldwide Headquarters

800 Enterprise Road, Suite 200

Horsham, PA 19044-3595, USA

Phone: +1 215 442 6100

Fax: +1 215 442 6199

E-Mail: dia@diahome.org