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Tailored Training

Optimise your training budget!
Save travel time. Save costs.
We will bring our expertise to you.

We will bring our expertise to you - where you need it, when you need it, tailored to your requirements.


DIA Tailored Training is a highly flexible, efficient and cost-effective way to get the maximum return on your training investment. Schedule your training course when it suits you best, at the venue of your choice. You can even adapt the content to include areas specific to your environment, and to match the level of expertise of the audience.

DIA Tailored Training is available to both public and private institutions and is delivered by instructors with no conflict of interest. The DIA Tailored Training programmes in Europe make the most of a selection of world-class expert faculty who are experienced professionals in the pharmaceutical and related industries.

DIA Europe offers Tailored Training Courses in:

  • Chemistry, Manufacturing and Controls (CMC) / Quality
  • Clinical Research
  • Non-Clinical Safety Sciences
  • Regulatory Affairs
  • Safety and Pharmacovigilance

Please contact Junes.Babay@diaeurope.org to discuss details - telephone: +41 61 225 51 54.

Please select from the rows below to display course details.

In-Company Training 

Title
Advanced Clinical Statistics for Nonstatisticians 10386
Art of Writing a Clinical Overview 24458
Clinical Project Management 13242
Clinical Statistics for Nonstatisticians 10381
CRO - Clinical Vendor Oversight: Vendor Life Cycle Management for Quality and Performance 2124278
Developing Standard Operating Procedures 10380
Development of a Clinical Study Report 10379
Electronic Submissions: The Next Era of Electronic Submissions 2526234
Enterprise Resource Management 16489
Essentials of European Regulatory Affairs 10377
Essentials of Project Management 10308
Executing and Controlling Biopharmaceutical Projects 11335
Fundamentals of Clinical Research Monitoring 10376
Fundamentals of Project Management for the Nonproject Manager 10309
Global Considerations for Regulatory Strategy Development 30108
Good Clinical Practices for the Clinical Research Professional 10375
High Performance Biopharm Teams 14215
How to Prepare for a Safety Inspection 20691
Introduction to Clinical Data Management 10382
Introduction to Computer Systems Validation 19537
Introduction to Portfolio Management and Performance Metrics 16188
Introduction to Signal Detection and Data Mining 20694
Medical Approach in Diagnosis and Management of ADRs 11120
Navigating Chemistry, Manufacturing and Controls through the Drug Development Process 19367
New Drug Product Development and Life Cycle Management 13461
Oversight of Clinical Monitoring: Trends and Strategies 13871
Overview of Drug Development 10310
Overview of Drug Development in Japan 12679
Postmarketing Drug Safety and Pharmacovigilance 21684
Pragmatic Approaches to Drug Safety Across the Premarketing and Postmarketing Continuum 29675
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
Regulatory Affairs for Biologics 21649
Regulatory Affairs Part I: The IND Phase 10307
Regulatory Affairs Part II: The NDA Phase 10306
Regulatory Affairs: The IND, NDA, and Postmarketing 10305
Risk Management and Safety Communication Strategies 22320
Strategies for Good Clinical Practice Audits 10374