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In-Person Instruction

DIA Professional
Development for
a Global Audience


DIA’s highly rated instructor-led training program is designed to inform and educate professionals and experts on critical issues related to pharmaceuticals, biotechnology, and medical products. With a myriad of training courses spanning the medical product life cycle, DIA’s training program provides professionals from industry, government, and academia with the opportunity to exchange ideas, knowledge, and best practices with peers and expert instructors. Courses offered range from European regulatory affairs to drug development to safety inspection preparation. In addition to expert instruction, each course offers interactive learning and small group exercises, as well as provides each participant with a comprehensive set of materials.

Additionally, DIA offers a professional development curriculum and certificate program in four interest areas:

Learn more about how to enroll in one of these Certificate Programs and continue on your professional development journey. Whether you are new to this industry, considering a career change, or just need a refresher, DIA has a course that will meet your professional development needs.

Review the list of courses below for more information and for future offerings. Each course also identifies its level as outlined below:

          Content is at an introductory level and provides the fundamental and essential knowledge of the topic area. Courses are appropriate for individuals new to the topic, looking for a career change, or a refresher on subject matter.
          Courses are for individuals who already have some knowledge of the topic area and are looking to enhance their skills and competence in the subject matter.
          Courses are for experienced individuals who have an in-depth knowledge of the subject matter or who have completed the basic or intermediate level courses. Content will focus on more complex issues.

Register today for DIA’s training courses and discover why these innovative professional development forums are valued by a growing global audience of pharmaceutical, biotechnology, medical device, and other professionals.

Contact Customer Service if you need additional information or if you have any questions.  

Instructor-Led Courses 

A Comprehensive Review of Regulatory Procedures for INDs/NDAs in the US 11122
Adaptive Design in Clinical Trials: When and How to Apply 3474872
Advanced GCP Study Monitoring 24056
Advanced Signal Detection - Tools, Triage, Evaluation, and Escalation 3443006
Advanced Workshop on QPPV Tool Box - Your Key to Success 6258303
An Introduction to Product Information Management 17118
Art of Writing a Clinical Overview 24458
Basics of the IND Phase 10307
Basics of the NDA Phase 10306
Benefit-Risk Management 29255
Biosimilar Development: Strategies and Regulatory Requirements for Global Market Entry 2686219
Building the eCTD: Practical Solutions to Compile Electronic Submissions 14773
Clinical Aspects of Quality Risk Management and Quality by Design 2088939
Clinical Project Management 13242
Clinical Project Management in Europe 20842
Clinical Statistics for Nonstatisticians 10381
Clinical Trial Audits in Practice 11095
Clinical Trial Management Essentials 15325
Comprehensive Training on European Regulatory Affairs including Different Registration Procedures and Variations: Expert Overview 17165
Developing Standard Operating Procedures 10380
Development of a Clinical Study Report 10379
Diagnosis and Management of Drug-Induced Liver Injury (DILI): Clinical Trials and Post-Marketing 2162769
Drug Safety and Pharmacovigilance Across the Product Lifecycle 29675
Electronic Submissions: The Next Era of Electronic Submissions 2526234
Enterprise Resource Management 16489
Essentials and Overview of the Regulatory Framework in Europe 10377
Essentials of Project Management 10308
EU Health Authorities Scientific and Regulatory Advice 6475737
EU Regulation of In-Vitro Diagnostics 3170749
EU-RMP Creation 6444309
European Regulatory Affairs: Keeping Your Finger on the Pulse of Marketing Authorizations 4005534
Excellence in Pharmacovigilance: Clinical Trials and Post-Marketing 14767
Executing and Controlling Biopharmaceutical Projects 11335
Fundamentals of Clinical Research Monitoring 10376
Fundamentals of Project Management for the Nonproject Manager 10309
Global CTD Dossier – Regulatory aspects and focus on quality documentation including concepts of Quality by Design 20794
Global Regulatory Strategy and Drug Development in Asia-Pacific, Latin America and Other Emerging Markets 30108
Good Clinical Practices for the Clinical Research Professional 10375
High Performance Biopharm Teams 14215
How to Manage a Successful Health Authority Interaction? 2088953
How to Prepare for a Safety Inspection 20691
How to Prepare for Pharmacovigilance Audits and Inspections in Europe 21617
HTA for Non-HTA User 27760
Innovative Statistical Approaches for Clinical Trials 10386
Introduction to Computer Systems Validation 19537
Introduction to Portfolio Management and Performance Metrics 16188
Introduction to Signal Detection and Data Mining 20694
Medical Affairs Training 5695546
Medical Approach in Diagnosis and Management of ADRs 11120
Medical Devices: Regulation and lifecycle management 23033
Medical Writing of Periodic Safety Update Reports (PSUR/PBRER) 6444317
Navigating Chemistry, Manufacturing and Controls through the Drug Development Process 19367
New Drug Product Development and Life Cycle Management 13461
Non-Clinical Safety Sciences and Their Regulatory Aspects 17110
Oversight of Clinical Monitoring: Trends and Strategies 13871
Overview of Drug Development 10310
Overview of Drug Development in Japan 12679
Paediatric Investigation Plans (PIP) 29280
Post-Authorisation Studies 3321889
Postmarketing Drug Safety and Pharmacovigilance 21684
Practical Guide for Pharmacovigilance: Clinical Trials and Post Marketing 17166
Pre-Marketing Clinical Safety 2164753
Premarketing Clinical Safety and Pharmacovigilance 21656
Preparing for a US FDA Advisory Committee Meeting 28296
Project Information, Communication, and Knowledge Management 16153
Project Risk Management 16145
Proven Strategies for Creating an Effective Clinical Research Program 28775
Quality by Design - Quality by Design - New concepts for Chemical and Biotech Product Development and Optimisation 23689
Regulatory Affairs for Biologics 21649
Regulatory Affairs for Combination Products 7121981
Regulatory Affairs: The IND, NDA, and Postmarketing 10305
Risk Management and Safety Communication Strategies 22320
Signal Management in Pharmacovigilance 21608
Strategies for Good Clinical Practice Audits 10374
The Basics of Clinical Data Management From Start to End 10382
The Development of Biopharmaceuticals - The Big Picture, Innovation and Scientific Requirements 26005
The Impact of Regulatory Affairs on Chemistry, Manufacturing & Controls (CMC) 29401
The Leadership Experience 10311
Training Course for eCTD Submissions in Switzerland 23714