Courses & programmes

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

Where does new knowledge, motivation and career development come from? At Atrium we have offered competence development for you in the life science sector for 50 years.  

Every year approx. 2,000 course participants get knowledge and skills updates with us and expand their professional network.

We are experts at engaging experts to teach at our courses.

This means you’ll meet both Danish and international capacities at Atrium – all specialists in their field.

As part of Lif (Lægemiddelindustriforeningen), we are close to both industry and the healthcare system, and we channel our insights into our courses to guarantee their relevance for you.

All in all, we believe lifelong learning is the root of new knowledge, motivation and a way to realise the career path of your choice.

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Individual courses
Adverse Drug Reactions by Body Systems

Module 7 Read more

Currently available on:

  • 11. Oct 2022
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:

  • 10. Nov 2021
Anatomy and physiology

Learn about the human body and its physiological functions Read more

Currently available on:

  • 8. Mar 2022
  • 4. Oct 2022
Audits and Inspections

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

Currently available on:

  • 9. Feb 2022
Biopharmaceuticals - Quality Development and Documentation

Module 10 Read more

Currently available on:

  • 15. Nov 2021
  • 30. Nov 2022
Clinical Development and Documentation

Module 8 Read more

Currently available on:

  • 25. Oct 2022
Clinical Project Management – Lead your project team

Module 2: Lead your clinical development project team Read more

Currently available on:

  • 17. Nov 2021
  • 20. Jun 2022
Clinical Project Management - Manage your project

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

Currently available on:

  • 30. Mar 2022
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:

  • 14. Dec 2021
  • 13. Dec 2022
Contracts in Clinical Trials

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

Currently available on:

  • 9. Jun 2022
Create value with 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:

  • 7. Dec 2021
  • 1. Nov 2022
Cross-Functional Market Access

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

Currently available on:

  • 2. Nov 2021
  • 3. May 2022
  • 25. Oct 2022
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:

  • 14. Mar 2022
  • 26. Sep 2022
Diploma in Vendor Management and oversight (module 1)

Obtain knowledge of best industry practices for clinical vendor management (module 1 of 2) Read more

Currently available on:

  • 24. Jan 2022
Diploma in Vendor Management and Oversight (module 2)

Obtain knowledge of best industry practices for Clinical Vendor Management and Oversight (module 2 ... Read more

Currently available on:

  • 25. Apr 2022
External Stakeholder Communication

Keep your external communication compliant with rules and regulations Read more

Currently available on:

  • 26. Apr 2022
Global Regulatory Strategies

Module 5 Read more

Currently available on:

  • 21. Sep 2022
Individual Case Safety Reports (ICSRs) - from narrative writing to causality assessment

Learn to structure a narrative that supports the reported adverse event and the causality assessment Read more

Currently available on:

  • 3. May 2022
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:

  • 11. Nov 2021
  • 9. Nov 2022
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:

  • 2. Nov 2021
  • 17. May 2022
  • 1. Nov 2022
Introduction to Market Access

For commercial and Medical Affairs professionals on the Danish market. Read more

Currently available on:

  • 22. Mar 2022
  • 5. Oct 2022
Introduction to Personalised Medicine

Learn the basics about potential and principles in genetically based treatments Read more

Currently available on:

  • Available online any time
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:

  • 28. Oct 2021
  • 28. Apr 2022
  • 3. Nov 2022
Market Access Management and Regulations

Learn how pharmaceuticals gain access to the Danish market Read more

Currently available on:

  • 21. Feb 2022
  • 5. Sep 2022
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:

  • 1. Dec 2021
  • 28. Sep 2022
Marketing Compliance: Digital Media

Learn the rules and legislation concerning communication about medicine on social and digital media Read more

Currently available on:

  • 30. Nov 2021
  • 18. May 2022
Medical Devices - Drug/Device Combinations

Module 12 Read more

Currently available on:

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

    GS1 standards for identification in clinical trials Read more

    Currently available on:

      Non-clinical Development and Documentation

      Module 7 Read more

      Currently available on:

      • 8. Dec 2021
      • 23. Nov 2022
      Optimizing Medical Writing for the Regulatory Reader

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

      Currently available on:

      • 1. Jun 2022
      Pathology

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

      Currently available on:

      • 8. Mar 2022
      • 4. Oct 2022
      Pathways to faster medicine approval

      Get an overview of established and new pathways in the EU, UK and US Read more

      Currently available on:

      • 5. Nov 2021
      Personalisierte Medizin

      Patienten haben ein Recht auf eine optimale und wirksame Behandlung mit einem minimalen Risiko von ... Read more

      Currently available on:

      • Available online any time
      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:

      • 17. Mar 2022
      • 15. Sep 2022
      Pharma Advertising and Interaction (Advanced)

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

      Currently available on:

      • 28. Oct 2021
      • 5. May 2022
      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. Mar 2022
      • 22. Sep 2022
      Pharmacoepidemiology Methods in Real World Evidence & Pass Studies

      Module 3 Read more

      Currently available on:

      • 5. Apr 2022
      Pharmacology I

      Kinetics and Dynamics Read more

      Currently available on:

      • 15. Mar 2022
      • 13. Sep 2022
      Pharmacology II

      Management and Surveillance Read more

      Currently available on:

      • 26. Oct 2021
      • 5. Apr 2022
      • 11. Oct 2022
      Pharmacology III

      Cases and Transfer Read more

      Currently available on:

      • 24. Nov 2021
      • 17. May 2022
      • 15. Nov 2022
      Pharmacovigilance Data in Application and Registration

      Understand the relationship between pharmacovigilance and the processes of application and ... Read more

      Currently available on:

      • 22. Mar 2022
      Pharmacovigilance Systems Master File

      Module 2 Read more

      Currently available on:

      • 10. Nov 2021
      Post-Marketing Surveillance

      Module 4 Read more

      Currently available on:

        Preclinical and Clinical Aspects of Pharmacovigilance

        Module 5 Read more

        Currently available on:

        • 15. Nov 2022
        Principles of Pharmacovigilance

        Module 1 Read more

        Currently available on:

        • 1. Feb 2022
        Product Life Cycle Activities

        Module 9 Read more

        Currently available on:

        • 9. Mar 2022
        Promotion in the Nordics

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

        Currently available on:

        • 18. Nov 2021
        • 24. Nov 2022
        QALY - DEEP DIVE INTO THE ECONOMIC MODELS

        Covering critique of models, communication of results and pricing strategies Read more

        Currently available on:

          Quality - Drug Substance and Drug Product

          Module 6 Read more

          Currently available on:

          • 2. Feb 2022
          Rethinking the future of Medical Affairs

          Adapt to the new pharmaceutical landscape focusing on innovation and cross-functional collaboration Read more

          Currently available on:

          • 16. Nov 2021
          Sales Intelligence

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

          Currently available on:

          • 28. Sep 2022
          Securing Market Uptake

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

          Currently available on:

          • 7. Jun 2022
          • 22. Nov 2022
          The EU Regulatory Environment - Procedures and Applications

          Module 2 Read more

          Currently available on:

          • 7. Sep 2022
          The Pharmaceutical Law Frameworks in the EU

          Module 1 Read more

          Currently available on:

          • 7. Feb 2022
          • 5. Oct 2022
          The Regulatory Affairs Environment for Generic Products in the EU

          Module 15 Read more

          Currently available on:

          • 19. Jan 2022
          The Regulatory Affairs Environment in Japan

          Module 4 Read more

          Currently available on:

          • 4. May 2022
          The US Regulatory Environment

          Module 3 Read more

          Currently available on:

          • 8. Jun 2022
          Understand the QALY method

          How quality-adjusted life years can be used to value health Read more

          Currently available on:

            Understanding Pharma

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

            Currently available on:

            • 2. Mar 2022
            • 7. Sep 2022
            Understanding Pharma

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

            Currently available on:

            • 8. Dec 2021
            Using Evidence

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

            Currently available on:

            • 7. Dec 2021
            • 1. Jun 2022
            • 30. Nov 2022
            seminars
            Exams
            Exam Adverse Drug Reactions by Body Systems (Online)

            Currently available on:

            • 10. Nov 2022
            Exam Diploma in ICH-GCP Managed trials (Online)

            Currently available on:

            • 8. Apr 2022
            • 28. Oct 2022
            Exam Diploma in Vendor management and oversight

            Currently available on:

            • 20. May 2022
            Exam Global Regulatory Strategies (Online)

            Currently available on:

            • 31. Oct 2022
            Exam Market Access

            Currently available on:

            • 23. Jun 2022
            Exam Marketing Compliance (Online)

            Currently available on:

            • 7. Apr 2022
            • 6. Oct 2022
            Exam Medical Devices - Drug/Device Combinations
            Exam Non-clinical Development and Documentation (Online)

            Currently available on:

            • 11. Jan 2022
            • 31. Jan 2023
            Exam Pharmacovigilance Data in Application and Registration (Online)

            Currently available on:

            • 27. Apr 2022
            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:

            • 15. Dec 2022
            Exam Principles of Pharmacovigilance (Online)

            Currently available on:

            • 4. Mar 2022
            Exam Product Life Cycle Activities (Online)

            Currently available on:

            • 8. Apr 2022
            Exam The Pharmaceutical Law Frameworks in the EU (Online)

            Currently available on:

            • 7. Mar 2022
            • 7. Nov 2022
            Exam The Regulatory Affair Environment in Japan

            Currently available on:

            • 3. Jun 2022
            Exam The Regulatory Affairs Environment for Generic Products in The EU (Online)

            Currently available on:

            • 10. Feb 2022
            Merit eksamen: Pathology

            Currently available on:

            • 10. Dec 2021
            Merit eksamen: Pharmacology I+II+III (online)

            Currently available on:

            • 10. Dec 2021
            Merit-eksamen: Anatomy and physiology

            Currently available on:

            • 10. Dec 2021
            Educational programmes
            CLINICAL PROJECT MANAGEMENT DIPLOMA

            A clinical 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
            Clinical Development Network

            A professional network on the recruitment and retention of patients in clinical trials Read more

            Currently available on:

            • 25. Nov 2021
            Marketing Compliance Network

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

            Currently available on:

            • 29. Sep 2021
            Regulatory Networking Group

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

            Currently available on:

            • 24. Jun 2021
            Events
            Afternoon meeting about risk situation medicines

            Do you know what to do? Get inspired by good practices from both primary and secondary care Read more

            Currently available on:

              Create results with Twitter and LinkedIn in life science

              Learn about target groups, language and algorithms. Read more

              Currently available on:

                Digital health – changing Pharma for good

                Towards improved disease prevention, diagnostics and treatment Read more

                Currently available on:

                • 1. Nov 2021
                Morning briefing: outsourcing in clinical trials

                Pitfalls and challenges when clinical trials are outsourced Read more

                Currently available on:

                  Pharma Debat

                  Debate and network for pharma professionals Read more

                  Currently available on:

                    The role of patient preferences in Market Access

                    Learn how HTAs, HCPs and patients’ associations value patient preferences Read more

                    Currently available on:

                    • 10. Nov 2021

                    Can’t find the course that meets your needs?

                    We can tailor a course exactly to the expertise and qualifications you are looking for. Give us a call to talk to one of our course experts.

                    Call +45 39 27 60 60 Monday-Friday 9:00-16:00 CET
                    Learn about tailored courses