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Clinical Safety & Pharmacovigilance Portal

This one-stop resource provides you with the comprehensive knowledge resources in regulatory affairs 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:

  • US and European regulatory affairs
  • Preparing for FDA meetings 
  • Post-approval regulatory requirements 
  • Regulatory requirements for product labeling & advertising 
  • Biologic products
  • Regulatory strategy
  • Quality assurance 
Meetings
   
magnifying glass DIA’s Annual Canadian Meeting
October 28-29 | Ottawa, ON, Canada
NA_14009
Patient Engagement throughout the Full Spectrum of Drug Development: An Interactive Workshop for Life Science Companies and Patient Groups
October 29-30 | Washington, DC
baby Pediatric Research Conference 2014
November 6-7 | Washington, DC
NA_15002
Pharmacovigilance and Risk Management Strategies 2015
January 26-28 | Washington, DC
   
In-Person Instruction
   
Training Pragmatic Approaches to Drug Safety Across the Premarketing and Postmarketing Continuum
August 18-20 | Horsham, PA
Training Clinical Project Management
August 18-19 | Horsham, PA
Training New Drug Product Development and Life Cycle Management
August 18-19 | Horsham, PA
Training Project Risk Management
August 20-21 | Horsham, PA
Training Development of a Clinical Study Report
September 15 | Rockville, MD
Training Clinical Statistics for Nonstatisticians
September 15 | Rockville, MD
Training Postmarketing Drug Safety and Pharmacovigilance
October 20-21 | Horsham, PA
Training Advanced Signal Detection - Tools, Triage, Evaluation, and Escalation
November 3-4 | Washington, DC
Training Risk Management and Safety Communications
November 10-11 | Bethesda, MD
   
Online Learning
   
Webinar Seven-Part Pediatric Drug Development Webinar Series - Part IV: Dosing in Children
July 08
Webinar Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 1: Fundamentals of Clinical Pharmacology: Pharmacokinetics
July 10
Online Training Advanced Clinical Statistics for Nonstatisticians
July 15-17 & 22-23
Online Training Adverse Event Reporting Requirements: IND and Postmarketing
July 22-24
Webinar Pharmacovigilance and Global Harmonization Updates
July 21
Webinar Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 2: Fundamentals of Clinical Pharmacology: Pharmacodynamics
August 7
Webinar Seven-Part Pediatric Drug Development Webinar Series - Part V: Technical Development: Pediatric Formulations
August 12
Webinar Five-Part Series on Fundamentals of Clinical Pharmacology For Drug Development - Part 3: Principles of Modeling and Simulation
September 4
Webinar Seven-Part Pediatric Drug Development Webinar Series - Part VI: Pre-clinical Toxicology & Safety
September 9
Online Training Art of Writing a Clinical Overview
September 9-11
Webinar Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 4: Determining the Safe First Human Dose
October 9
Webinar Seven-Part Pediatric Drug Development Webinar Series - Part VII: Operational Challenges of Pediatric Clinical Trials
October 14
Webinar Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 5: Assessment of QT Prolongation
November 6
   
Resources
   
eLearning
View complete catalogue of eLearning Modules. 
   

Get the Big Picture of DIA’s Training Offerings:

"Safety Resource Video"