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Individual courses
Adverse Drug Reactions by Body Systems

Module 7 Read more

Currently available on:

  • 15. Mar 2021
Agile Fundamentals and the Scrum Framework

Would you like to learn what ‘agile’ really is and how to use it in your professional role? Read more

Currently available on:

  • 4. Nov 2020
  • 10. Nov 2021
Anatomy and physiology (blended learning)

Learn about the human body and its physiological functions Read more

Currently available on:

  • 10. Mar 2021
  • 7. Sep 2021
Biopharmaceuticals - Quality Development and Documentation

Module 10 Read more

Currently available on:

  • 5. Oct 2020
  • 22. Jun 2021
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

Clinic/Industry collaboration for implementation of advanced immune therapies

Debate about collaboration for the total treatment Read more

Currently available on:

  • 26. Nov 2020
Clinical Development and Documentation

Module 8 Read more

Currently available on:

  • 28. Sep 2020
Clinical Project Management – Lead your project team

Module 2: Lead your clinical development project team Read more

Currently available on:

  • 25. Nov 2020
  • 21. Apr 2021
Clinical Project Management - Manage your project

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

Currently available on:

  • 26. Oct 2020
  • 22. Mar 2021
Clinical Trial Risk Management In Practice

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

Currently available on:

  • 7. Dec 2020
Contracts in Clinical Trials

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

Currently available on:

  • 3. Jun 2021
Cross-Functional Market Access

Learn how you can improve your market access activities through cross-functional collaboration Read more

Currently available on:

  • 4. May 2021
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

Currently available on:

  • 22. Sep 2020
  • 10. Mar 2021
  • 1. Sep 2021
Do's and don'ts in virtual meetings (online course)

“Do's and don'ts in virtual meetings” is open to anyone who wants a basic understanding of how to ... Read more

Currently available on:

  • 30. Sep 2020
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:

  • 10. Nov 2020
Global Regulatory Strategies

Module 5 Read more

Currently available on:

  • 14. Sep 2021
ICH-GCP Refresher Training Course

Are you compliant and updated on ICH-GCP and the R2 headlines? Read more

Introduction to Clinical development

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

Currently available on:

  • 3. Nov 2020
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:

  • 26. Oct 2020
Introduction to Marketing Compliance in the Pharma Industry

Get an introduction to ENLI and the pharmaceutical industry’s self-regulation and avoid common and ... Read more

Currently available on:

  • 24. Nov 2020
Introduction to Regulatory Affairs

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

Currently available on:

  • 10. Nov 2020
  • 26. Apr 2021
Market Access Management and Regulations

Learn how pharmaceuticals gain access to the Danish market Read more

Currently available on:

  • 24. Mar 2021
Market Access Today and Tomorrow

Understand the frameworks that market access operates in and learn how you stay at the forefront of ... Read more

Currently available on:

  • 25. Nov 2020
  • 1. Dec 2021
MCA 1: Pharma Advertising and Information (Basic)

Learn the Danish laws and rules on information for healthcare professionals (HCPs) and the public Read more

Currently available on:

  • 2. Oct 2020
  • 16. Mar 2021
  • 21. Sep 2021
MCA 2: Pharma Interaction (Basic) – Meeting and Training HCPs

Learn the Danish laws and rules on interacting with healthcare professionals (HCPs) Read more

Currently available on:

  • 24. Sep 2020
  • 23. Mar 2021
  • 28. Sep 2021
MCA 3: Pharma Advertising and Interaction (Advanced)

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

Currently available on:

  • 27. Oct 2020
  • 2. Nov 2021
MCA 4: External Stakeholder Communication

Keep your market access and public affairs activities compliant when dealing with patient ... Read more

Currently available on:

  • 20. Jan 2021
MCA 5: Promotion in the Nordics

Pharmaceutical marketing compliance in Sweden, Norway, Finland and Denmark Read more

Currently available on:

  • 28. Jan 2021
  • 18. Nov 2021
MCA 6: Marketing Compliance: Digital Media

Learn the rules and legislation concerning online communication, social media, apps and devices in ... Read more

Currently available on:

  • 25. Nov 2020
  • 19. May 2021
Medical Devices - Drug/Device Combinations

Module 12 Read more

New standards for Investigational Medicinal Products (IMP) in clinical trials (online)

GS1 standards for identification in clinical trials Read more

Currently available on:

  • 21. Oct 2020
Non-clinical Development and Documentation

Module 7 Read more

Currently available on:

  • 30. Nov 2020
Optimizing Medical Writing for the Regulatory Reader

Learn how you handle challenges when you write or revise regulatory documents Read more

Currently available on:

  • 17. May 2021
Pathology (blended learning)

Learn about the most common diseases in humans, the causes and symptoms, and the recommended ... Read more

Currently available on:

  • 10. Mar 2021
  • 7. Sep 2021
Pharmacoepidemiology Methods in Real World Evidence & Pass Studies

Module 3 Read more

Currently available on:

  • 4. May 2021
Pharmacology I

Kinetics and Dynamics Read more

Currently available on:

  • 17. Mar 2021
  • 14. Sep 2021
Pharmacology II

Management and Surveillance Read more

Currently available on:

  • 20. Oct 2020
  • 20. Apr 2021
  • 26. Oct 2021
Pharmacology III

Cases and Transfer Read more

Currently available on:

  • 17. Nov 2020
  • 26. May 2021
  • 24. Nov 2021
Pharmacovigilance Data in Application and Registration

Module 6 Read more

Pharmacovigilance Systems Master File

Module 2 Read more

Currently available on:

  • 9. Nov 2021
Post-Marketing Surveillance

Module 4 Read more

Currently available on:

  • 5. Oct 2021
Preclinical and Clinical Aspects of Pharmacovigilance

Module 5 Read more

Currently available on:

  • 8. Mar 2022
Principles of Pharmacovigilance

Module 1 Read more

Currently available on:

  • 21. Oct 2020
Product Life Cycle Activities

Module 9 Read more

Currently available on:

  • 18. Jan 2021
Quality - Drug Substance and Drug Product

Module 6 Read more

Currently available on:

  • 8. Dec 2020
Sales Intelligence

Learn about the key theories used for analyzing markets and how to use market data Read more

Currently available on:

  • 29. Sep 2020
  • 13. Apr 2021
  • 5. Oct 2021
Securing Market Uptake

Learn whom to talk to when, why and how Read more

Currently available on:

  • 6. Oct 2020
  • 12. Oct 2021
Site Audits and Inspections

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

Currently available on:

  • 24. Nov 2020
Statistics and evidence in relation to the Medicines Council (Online course)

Through lectures, interactive dialogue and practical assignments, the student is guided through ... Read more

Systematic Innovation in Pharma

In this course, you will be introduced to the new ISO standard for Innovation Management. Read more

Currently available on:

  • 24. Feb 2021
The EU Regulatory Environment - Procedures and Applications

Module 2 Read more

The Pharmaceutical Law Frameworks in the EU

Module 1 Read more

Currently available on:

  • 18. Nov 2020
The Regulatory Affairs Environment for Generic Products in the EU

Module 15 Read more

Currently available on:

  • 8. Oct 2020
The Regulatory Affairs Environment in Japan

Module 4 Read more

The US Regulatory Environment

Module 3 Read more

Currently available on:

  • 1. Mar 2021
Understand the QALY method - just as well as the Danish Medicines Council

From added value to quality-adjusted life years Read more

Currently available on:

  • 10. Nov 2020
  • 26. Jan 2021
Understanding Pharma

Get the competences to start a successful career in the pharmaceutical industry Read more

Currently available on:

  • 2. Mar 2021
  • 1. Sep 2021
Using Evidence

Learn how to critically process and analyse medical scientific literature Read more

Currently available on:

  • 8. Dec 2020
  • 1. Jun 2021
  • 7. Dec 2021
Veterinary Pharmacovigilance

Module 8 Read more

Currently available on:

  • 8. Sep 2021
Exams
Exam Adverse Drug Reactions by Body Systems (Online)

Currently available on:

  • 7. Dec 2020
Exam Diploma in ICH-GCP Managed trials (Online)

Currently available on:

  • 19. Oct 2020
  • 9. Apr 2021
  • 1. Oct 2021
Exam Global Regulatory Strategies (Online)

Currently available on:

  • 14. Oct 2021
Exam Marketing Compliance (Online)

Currently available on:

  • 22. Oct 2020
  • 7. Apr 2021
  • 14. Oct 2021
Exam Medical Devices - Drug/Device Combinations
Exam Non-clinical Development and Documentation (Online)

Currently available on:

  • 12. Jan 2021
Exam Pharmacoepidemiology

Currently available on:

  • 3. Jun 2021
Exam Pharmacovigilance Data in Application and Registration (Online)

Currently available on:

  • 7. Oct 2020
Exam Pharmacovigilance Systems Master File (Online)

Currently available on:

  • 7. Dec 2021
Exam Post-Marketing Surveillance (Online)

Currently available on:

  • 4. Nov 2021
Exam Preclinical and Clinical Aspects of Pharmacovigilance

Currently available on:

  • 5. Apr 2022
Exam Principles of Pharmacovigilance (Online)

Currently available on:

  • 16. Nov 2020
Exam Product Life Cycle Activities (Online)

Currently available on:

  • 9. Feb 2021
Exam The Pharmaceutical Law Frameworks in the EU (Online)

Currently available on:

  • 16. Dec 2020
Exam The Regulatory Affair Environment in Japan
Exam The Regulatory Affairs Environment for Generic Products in The EU (Online)

Currently available on:

  • 12. Nov 2020
Exam Veterinary Pharmacovigilance (Online)

Currently available on:

  • 4. Mar 2021
Merit eksamen: Pathology
Merit eksamen: Pharmacology I+II+III (online)

Currently available on:

  • 3. Dec 2020
Merit-eksamen: Anatomy and physiology
Educational programmes
CLINICAL PROJECT MANAGEMENT DIPLOMA

A project management programme for professionals in clinical development Read more

Market Access Programme

The latest practical tools and information Read more

Marketing Compliance Programme

Understanding ethical standards in pharmaceutical marketing Read more

Master of Medicines Regulatory Affairs (MRA)

University of Copenhagen in collaboration with Atrium Read more

Pharma Business Programme

Get an all-round understanding of pharmaceutical business decisions: From identifying USPs and ... Read more

Pharma Consultant Programme

Conceptual knowledge that is necessary for success in the pharma industry Read more

Pharmacovigilance Diploma

An international training programme Read more

Regulatory Affairs Diploma

Theoretical and practical aspects Read more

Networks
Market access network

A network for professionals working with market access in a pharmaceutical company Read more

Marketing compliance network 2019/2020

A network for individuals working with marketing compliance in a pharmaceutical company Read more

Regulatory Networking Group

Join a professional community with colleagues from the industry and authorities Read more

seminars
EVALUATION OF MEDICINES IN DANISH HOSPITALS

From added value to QALY Read more

Currently available on:

  • 10. Dec 2020
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

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