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

Featured Event
	DIA 2013 49th Annual Meeting: Advancing Therapeutic Innovation and Regulatory Science  June 23-27 | Boston, MA
Meetings
	The Development of Live Biotherapeutics September 24 | Rockville, MD
	DIA/FDA Oligonucleotide-based Therapeutics Conference September 25-27 | Washington, DC
	Optimizing Expectations and Success in Support of First-in-Human Trials (FIH) with Stem Cell Therapies September 26-27 | Washington, DC
	Clinical Trial Disclosure: Towards a More Transparent World October 1-2 | Bethesda, MD
	US Conference on Rare Diseases and Orphan Products October 7-9 | North Bethesda, MD
	Drug-Induced Injury of Liver, Heart, Kidney, and Skin: Employing Recent Advances to Improve Patient Safety and Speed Up the Pipeline October 15-17 | North Bethesda, MD
	DIA's Annual Canadian Meeting: New Reality/New Frontiers October 29-30 | Ottawa, ON, Canada
	Pharmacovigilance and Risk Management Strategies 2014 January 13-15 | Washington, DC
In-Person Instruction
	Pragmatic Approaches to Drug Safety Across the Premarketing and Postmarketing Continuum August 12-14 | Boston, MA
	Regulatory Affairs: The IND, NDA, and Postmarketing August 12-15 | Boston, MA
	Clinical Project Management August 12-13 | Boston, MA
	New Drug Product Development and Life Cycle Management August 12-15 | Boston, MA
	Regulatory Affairs for Biologics September 23-24 | Horsham, PA
	Global Considerations for Regulatory Strategy Development October 17-18 | Horsham, PA
	Risk Management and Safety Communications Strategies November 4-5 | Horsham, PA
	Regulatory Affairs: The IND, NDA, and Postmarketing November 11-14 | Philadelphia, PA
	The Leadership Experience November 11-13 | Philadelphia, PA
Online Learning
	Drug & Cosmetic Rule Amendments: Changes in Regulations Governing Clinical Trials in India June 6
	Assessing the Benefits and Risks of Medicines: Webinar Series - Part 7: A Structured, Quantitative Health Outcomes Approach to Drug Benefit-Risk Analysis June 12
	Advanced Clinical Statistics for the Nonstatistician Begins July 16
	Interactions with the FDA During the IND/NDA Phases Begins July 23
	Assessing the Benefits and Risks of Medicines: Webinar Series- Part 8: Visualization and Communication of Benefit-Risk July 24
	Adverse Event Reporting Requirements: IND and Postmarketing Begins July 30
	Strategies for Good Clinical Practice Audits Begins September 9
	Planning and Managing Your Project Begins September 10
	Introduction to Clinical Data Management Begins September 17
	Change Management, Issues Management, Escalation Management September 18
	Basics of the IND Begins October 1
	Preparing a Clinical Trial Budget October 2
	Basics of the NDA Begins October 22
	Negotiation and Influence October 30
	Team Building and Development November 6
	Project Risk Management: Dealing with the Certainty of Uncertainty November 7
Resources
	View complete catalogue of eLearning Modules.
	View Clinical Research Brochure FDA Process Demystified by DIA Course Offerings, October 2011

Get the Big Picture of DIA’s Training Offerings: