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What Others Are Saying...

"Absolutely recommend...It explains a lot of the things that we deal with on a day-to-day basis in clinical study.”

--Donna Kipphorn, Manager, Regulatory Affairs at Janssen Pharmaceuticals

"I've learned more in the last two days than I thought was possible."

--Bill York, Safety Associate III at Otsuka Pharmaceutical Development & Commercialization

Clinical Research Portal

This one-stop resource provides you with the information and knowledge resources to help you develop skills and learn proven strategies and techniques to help you overcome the challenges you face in your profession.


This resource center addresses all of today’s hottest topics, including:

  • Good clinical practices
  • Fundamentals of clinical research monitoring 
  • Introduction to comparative  effectiveness research 
  • Clinical statistics for the nonstatisticians 
  • Development of a clinical study report
Meetings
 

 

NA_15008 DIA/FDA Statistics Forum 2015
April 20-22 | North Bethesda, MD
NA_15003 eRegulatory and Intelligence Annual Conference
May 11-13 | Philadelphia, PA
DIA Annual Meeting DIA 2015 51st Annual Meeting: Develop. Innovate. Advance.
June 14-18 | Washington, DC
DIA/FDA Oligonucleotide-based Therapeutic Conference 2015 DIA/FDA Oligonucleotide-based Therapeutic Conference 2015
September 9-11 | Washington, DC
 	Patient Engagement in Benefit-Risk Assessment throughout the Life Cycle of Medical Products Patient Engagement in Benefit-Risk Assessment throughout the Life Cycle of Medical Products
September 17-18 | North Bthesda, MD
NA 15012 Biosimilars
October 19-20 | Bethesda, MD
   
In-Person Instruction
   
Training Regulatory Affairs for Biologics
April 14-15 | Bethesda, MD
Training Advanced Signal Detection - Tools, Triage, Evaluation, and Escalation
April 20-21 | Washington, DC
Training Key Considerations for the Development and Marketing of Biosimilar Products
April 27-28 | Washington, DC
Training Pragmatic Approaches to Drug Safety Across the Premarketing and Postmarketing Continuum
April 29-May 1 | Washington, DC
Training Electronic Submissions: The Next Era of Electronic Submissions
May 14 | Philadelphia, PA
Training Global Regulatory Strategy and Drug Development in Asia-Pacific, Latin America and Other Emerging Markets
August 3-4 | Washington, DC
Training Pragmatic Approaches to Drug Safety Across the Premarketing and Postmarketing Continuum
August 10-12 | Boston, MA
Training Development of a Clinical Study Report
August 10 | Boston, MA
Training Regulatory Affairs: The IND, NDA, and Postmarketing
August 10-13 | Boston, MA
Training Clinical Project Management
August 24-25 | Washington, DC
Training New Drug Product Development and Life Cycle Management
August 26-27 | Washington, DC
Training Adaptive Design in Clinical Trials: When and How to Apply
September 14-15 | Washington, DC
Training Clinical Statistics for Nonstatisticians
September 28-29 | Washington, DC
Training Risk Management and Safety Communication
October 26-27 | Washington, DC
Training Regulatory Affairs: The IND, NDA, and Postmarketing
November 9-12 | Philadelphia, PA
Training Advanced Clinical Statistics for NonStatisticians
November 11-12 | Philadelphia, PA
   
Online Learning
   
Webinar GVP Module IX Compliant Signal Management Systems in Pharmacovigilance: A Tale of Two Experiences
April 2 | Online
Online Training Basics of the IND Phase
May 4-7 | Online
Online Training Oversight of Clinical Monitoring: Trends and Strategies
May 5-7 | Online
Online Training Basics of the NDA Phase
May 18-21 | Online
Online Training Adverse Event Reporting Requirements: IND and Post-marketing
July 13-15 | Online
Online Training Interactions with the FDA during IND/NDA Phases
July 16 | Online
Online Training Overview of Drug Development in Japan
September 2-3 & 9-10 | Online
Online Training Introduction to Signal Detection and Data Mining
October 5-8 | Online
   
Resources
   
eLearning
View complete catalogue of eLearning Modules. 

Get the Big Picture of DIA’s Training Offerings: