Courses & programmes

Choose from a range of single courses and seminars, or enrol in an educational programme.

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Individual courses
Adverse Drug Reactions by Body Systems

Module 7 Read more

Part of Pharmacovigilance Diploma

Currently available on:

  • 5. Nov 2018
Advertisements in the Nordic region

A Nordic Compliance Seminar Read more

Part of Marketing Compliance Academy

Currently available on:

  • 22. Nov 2018
Anatomy and Physiology (evening course)

Module 1 Read more

Part of Danish Pharmaceutical Academy

Anatomy and physiology (online course)

Module 1 Read more

Part of Danish Pharmaceutical Academy

Currently available on:

  • 31. Jul 2018
Anatomy and Physiology (weekend course)

Module 1 Read more

Part of Danish Pharmaceutical Academy

Currently available on:

  • 28. Sep 2018
Basic Regulatory Aspects of Clinical Development

Get a basic overview of clinical development Read more

Biopharmaceuticals - Quality Development and Documentation

Module 10 Read more

Part of Master of Medicines Regulatory Affairs (MRA) and Regulatory Affairs Diploma

Currently available on:

  • 3. Apr 2019
Certificate in Advanced Good Clinical Practice

Get up to date with the latest legislation and learn how to maintain a high standard of work in a ... Read more

Currently available on:

  • 19. Nov 2018
Certificate in Basic Good Clinical Practice

Get a basic understandig of ICH GCP Read more

Currently available on:

  • 29. Oct 2018
Clinical Development and Documentation

Module 8 Read more

Part of Master of Medicines Regulatory Affairs (MRA) and Regulatory Affairs Diploma

Currently available on:

  • 23. Apr 2019
Clinical Project Management – Lead your project team

Module 2: Lead your clinical development project team Read more

Currently available on:

  • 14. Jan 2019
Clinical Project Management - Manage your project

Module 1: Learn how to manage your clinical development project Read more

Currently available on:

  • 26. Nov 2018
Communication and advertising to healthcare professionals - advanced

Improve your knowledge of pharmaceutical advertising aimed at health care professionals Read more

Part of Marketing Compliance Academy

Currently available on:

  • 7. Nov 2018
Communication and advertising to healthcare professionals - basic

Get an introduction to the rules of the Ethical Committee for the Pharmaceutical Industry (ENLI) Read more

Part of Marketing Compliance Academy

Currently available on:

  • 6. Sep 2018
  • 4. Dec 2018
Communication and advertising to the public

Learn the fundamental rules concerning communicating and advertising pharmaceuticals to patients ... Read more

Part of Marketing Compliance Academy

Currently available on:

  • 17. Oct 2018
Communication with external stakeholders

Get an overview of the rules concerning communication with decision makers and other stakeholders Read more

Part of Marketing Compliance Academy

Contracts in Clinical Trials

Are you familiar with the legal rules and principles in contracts and the consequent requirements ... Read more

Diploma in ICH-GCP managed trials

Get a thorough understanding of ICH-GCP as well as the statutory and practical aspects of executing ... Read more

Part of Diploma in ICH-GCP managed trials

Currently available on:

  • 17. Sep 2018
eHealth - the pharmaceutical industry´s use of e-communication and apps

Learn the rules and legislation concerning eHealth as a marketing tool Read more

Part of Marketing Compliance Academy

Generation and value of Real World Evidence (RWE)

How can your company make use of the large amount of Real World Data available to generate evidence ... Read more

Currently available on:

  • 14. Nov 2018
Global Regulatory Strategies

Module 5 Read more

Part of Regulatory Affairs Diploma

Currently available on:

  • 4. Dec 2018
Introduction to Clinical Drug Research

This course provides you with a general overview and understanding of why we do clinical drug ... Read more

Currently available on:

  • 9. Oct 2018
Introduction to Drug Safety and Pharmacovigilance

Learn the terminology and the basic elements of drug safety and clinical trial safety Read more

Currently available on:

  • 8. Oct 2018
Introduction to Regulatory Affairs

Learn about the many tasks of a regulatory affairs department and how to obtain and maintain a ... Read more

Law, ethics and stakeholders

Module 3 Read more

Part of Danish Pharmaceutical Academy

Currently available on:

  • 1. Nov 2018
Market insight and mechanisms

Module 5 Read more

Part of Danish Pharmaceutical Academy

Currently available on:

  • 27. Nov 2018
Masterclass – GDPR for Pharma - from Theory to Practical Implementation

Get the tools to implement the new General Data Protection Regulation (GDPR) in your company Read more

Masterclass - Market Access process with The Danish Medicines Council

Grade methodology and practical experience Read more

Masterclass - Performance and presentation techniques

Learn how to impact your audience Read more

Currently available on:

  • 12. Sep 2018
Medical Devices - Drug/Device Combinations

Module 12 Read more

Part of Regulatory Affairs Diploma

Currently available on:

  • 4. Oct 2018
Medical evaluation of Individual Case Safety Reports (ICSRs)

Learn how to evaluate Individual Case Safety Reports (ICSRs) and prepare the ideal sender comment Read more

Currently available on:

  • 6. Dec 2018
Medical Market Access: Stakeholders and Influencers

Learn about the Danish healthcare system and get an overview of the relevant actors and stakeholders Read more

Part of Medical Market Access Diploma

Currently available on:

  • 4. Mar 2019
Medical Market Access: The Economic Decision-Makers

Get an overview of actors and decision-making processes and learn about relevant concepts and models Read more

Part of Medical Market Access Diploma

Medical Market Access: The Political Healthcare Sector

Get an overview of the political healthcare sector and learn about the actors who play a role in ... Read more

Part of Medical Market Access Diploma

Currently available on:

  • 30. Oct 2018
Non-clinical Development and Documentation

Module 7 Read more

Part of Regulatory Affairs Diploma

Currently available on:

  • 4. Feb 2019
Pathology (evening course)

Module 2 Read more

Part of Danish Pharmaceutical Academy

Pathology (online course)

Module 2 Read more

Part of Danish Pharmaceutical Academy

Currently available on:

  • 31. Jul 2018
Pathology (weekend course)

Module 2 Read more

Part of Danish Pharmaceutical Academy

Currently available on:

  • 7. Sep 2018
Pharmacoepidemiology

Module 3 Read more

Part of Pharmacovigilance Diploma

Pharmacology I (evening course)

Module 4 part 1 Read more

Part of Danish Pharmaceutical Academy

Pharmacology I (online course)

Module 4 part 1 Read more

Part of Danish Pharmaceutical Academy

Currently available on:

  • 31. Jul 2018
Pharmacology I (weekend course)

Module 4 part 1 Read more

Part of Danish Pharmaceutical Academy

Currently available on:

  • 14. Sep 2018
Pharmacology II

Module 4 part 2 Read more

Part of Danish Pharmaceutical Academy

Currently available on:

  • 5. Oct 2018
  • 27. Sep 2019
Pharmacovigilance Data in Application and Registration

Module 6 Read more

Part of Pharmacovigilance Diploma

Currently available on:

  • 19. Nov 2019
Pharmacovigilance Systems Master File

Module 2 Read more

Part of Pharmacovigilance Diploma

Pharmacovigilance Workshop in Zagreb

In collaboration with HALMED and the Croatian Pharmaceutical Society (HFD) Read more

Currently available on:

  • 1. Oct 2018
Post-Marketing Surveillance

Module 4 Read more

Part of Pharmacovigilance Diploma

Preclinical and Clinical Aspects of Pharmacovigilance

Module 5 Read more

Part of Pharmacovigilance Diploma

Principles of Pharmacovigilance

Module 1 Read more

Part of Pharmacovigilance Diploma

Currently available on:

  • 3. Oct 2018
Procedures and Applications in the EU

Module 2 Read more

Part of Master of Medicines Regulatory Affairs (MRA) and Regulatory Affairs Diploma

Currently available on:

  • 3. Sep 2018
Product Life Cycle Activities

Module 9 Read more

Part of Regulatory Affairs Diploma

Currently available on:

  • 27. Nov 2018
Quality - Drug Substance and Drug Product

Module 6 Read more

Part of Master of Medicines Regulatory Affairs (MRA) and Regulatory Affairs Diploma

Currently available on:

  • 8. Oct 2018
Reading Scientific Papers - Advanced

Learn how to analyze systematic literature studies and meta-analysis Read more

Reading Scientific Papers - Basic

Understand scientific studies and learn to recognize strengths and weaknesses of a study design Read more

Risk Management and Risk Based Monitoring in a Clinical Research Setting

Understand risk management principles and the links between study level risk management and the ... Read more

Site Audits and Inspections

Learn what it takes to be audit and inspection ready Read more

Currently available on:

  • 6. Nov 2018
Statistics for Non-statisticians

Understand the strengths and weaknesses behind the statistics of scientific literature Read more

Currently available on:

  • 20. Sep 2018
Status on Disease Treatment and Pharmaceuticals

Get an update on the latest knowledge in disease treatment and pharmaceuticals adjusted to ... Read more

Currently available on:

  • 21. Nov 2018
The Pharmaceutical Law Frameworks in the EU

Module 1 Read more

Part of Regulatory Affairs Diploma

The Regulatory Affair Environment in Japan

Module 4 Read more

Part of Regulatory Affairs Diploma

Currently available on:

  • 19. Mar 2019
The Regulatory Affair Environment in the USA

Module 3 Read more

Part of Master of Medicines Regulatory Affairs (MRA) and Regulatory Affairs Diploma

The Regulatory Affairs Environment for Generic Products in the EU

Module 15 Read more

Currently available on:

  • 15. Nov 2018
Understanding Pharma

Understand the value chain in the pharmaceutical industry from drug development to sales and ... Read more

Currently available on:

  • 2. Oct 2018
Veterinary Pharmacovigilance

Module 8 Read more

Part of Pharmacovigilance Diploma and Regulatory Affairs Diploma

Currently available on:

  • 28. Nov 2018
Veterinary Regulatory Affairs in the EU

Module 14 Read more

Currently available on:

  • 11. Sep 2018
Exams
Exam Adverse Drug Reactions by Body Systems

date: 5. Dec 2018

Exam Danish Pharmaceutical Academy: Anatomy and physiology

date: 13. Nov 2018

Exam Danish pharmaceutical academy: Law, ethics and stakeholders

date: 13. Nov 2018

Exam Danish Pharmaceutical Academy: Market insight and mechanisms

date: 29. Nov 2018

Exam Danish pharmaceutical academy: Pathology

date: 13. Nov 2018

Exam Danish pharmaceutical academy: Pharmacology I

date: 13. Nov 2018

Exam Danish pharmaceutical academy: Pharmacology II

date: 30. Oct 2018

Exam Diploma in ICH-GCP Managed trials

date: 23. Oct 2018

Exam Global Regulatory Strategies

date: 8. Jan 2019

Exam Marketing Compliance Academy

date: 22. Aug 2018

Exam Medical Market Access

date: 9. Nov 2018

Exam Non-clinical Development and Documentation

date: 8. Mar 2019

Exam Pharmacoepidemiology

date: 28. Aug 2017

Exam Pharmacovigilance Data in Application and Registration

date: 30. Oct 2017

Exam Pharmacovigilance Systems Master File

date: 26. Oct 2017

Exam Post-Marketing Surveillance

date: 4. Jun 2018

Exam Preclinical and Clinical Aspects of Pharmacovigilance

date: 27. Feb 2018

Exam Principles of Pharmacovigilance

date: 2. Nov 2018

Exam Product Life Cycle Activities

date: 18. Dec 2018

Exam TEST - B

date: 24. Dec 2018

Exam The Pharmaceutical Law Frameworks in the EU

date: 19. Jun 2018

Exam The Regulatory Affair Environment in Japan

date: 26. Apr 2019

Exam The Regulatory Affairs Environment for Generic Products in The EU

date: 30. Apr 2018

Exam Veterinary Pharmacovigilance

date: 3. Jan 2019

Exam Veterinary Regulatory Affairs in the EU

date: 11. Oct 2018

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