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Adverse Drug Reactions by Body Systems
Module 7 Read more
Agile Brand Planning
Learn how to deliver the brand plan the pharma industry expects and how to surpass their ... Read more
Anatomy and physiology (online course)
Learn about the human body and its physiological functions Read more
Currently available on:
- 10. Mar 2020
Audits and Inspections
Learn what it takes to be audit and inspection ready Read more
Basic Regulatory Aspects of Clinical Development
Get a basic overview of clinical development Read more
Biopharmaceuticals - Quality Development and Documentation
Module 10 Read more
Currently available on:
- 5. Oct 2020
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
Clinical Development and Documentation
Module 8 Read more
Currently available on:
- 21. Apr 2020
Clinical Project Management – Lead your project team
Module 2: Lead your clinical development project team Read more
Currently available on:
- 13. Jan 2020
Clinical Project Management - Manage your project
Module 1: Learn how to manage your clinical development project Read more
Currently available on:
- 11. Nov 2019
Contracts in Clinical Trials
Are you familiar with the legal rules and principles in contracts and the consequent requirements ... Read more
Cross-Functional Market Access
Learn how you can improve your market access activities through cross-functional collaboration Read more
Currently available on:
- 12. May 2020
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
External Stakeholder Communication
Keep your market access and public affairs activities compliant when dealing with patient ... Read more
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
Global Regulatory Strategies
Module 5 Read more
Currently available on:
- 15. Jan 2020
ICH-GCP Refresher Training Course
Are you compliant and updated on ICH-GCP and the R2 headlines? Read more
Introduction to Clinical development of New Medicine
This course provides you with a general overview and understanding of why and how we do clinical ... Read more
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:
- 22. Oct 2019
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:
- 25. Nov 2019
Market Access Management and Regulations
Learn how pharmaceuticals gain access to the Danish market Read more
Currently available on:
- 17. Mar 2020
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:
- 20. Nov 2019
Marketing Compliance: Digital Media
Learn the rules and legislation concerning online communication, social media, apps and devices in ... Read more
Currently available on:
- 16. Jun 2020
Medical Devices - Drug/Device Combinations
Module 12 Read more
Currently available on:
- 12. Mar 2020
Non-clinical Development and Documentation
Module 7 Read more
Currently available on:
- 15. Sep 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:
- 29. Oct 2019
Pathology (online course)
Learn about the most common diseases in humans, the causes and symptoms, and the recommended ... Read more
Currently available on:
- 10. Mar 2020
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:
- 5. Dec 2019
- 31. Mar 2020
Pharma Advertising and Interaction (Advanced)
Improve your knowledge of pharmaceutical advertising aimed at health care professionals Read more
Currently available on:
- 24. Oct 2019
Pharma Interaction (Basic) – Meeting and Training HCPs
Learn the Danish laws and rules on interacting with healthcare professionals (HCPs) Read more
Currently available on:
- 30. Oct 2019
- 12. Mar 2020
Pharmacoepidemiology Methods in Real World Evidence & Pass Studies
Module 3 Read more
Pharmacology I
Kinetics and Dynamics Read more
Currently available on:
- 25. Mar 2020
Pharmacology II
Management and Surveillance Read more
Currently available on:
- 22. Oct 2019
- 29. Apr 2020
Pharmacology III
Cases and Transfer Read more
Currently available on:
- 26. Nov 2019
- 27. May 2020
Pharmacovigilance Data in Application and Registration
Module 6 Read more
Currently available on:
- 19. Nov 2019
Pharmacovigilance Systems Master File
Module 2 Read more
Currently available on:
- 21. Jan 2020
Post-Marketing Surveillance
Module 4 Read more
Currently available on:
- 10. Dec 2019
Preclinical and Clinical Aspects of Pharmacovigilance
Module 5 Read more
Currently available on:
- 29. Jan 2020
Principles of Pharmacovigilance
Module 1 Read more
Product Life Cycle Activities
Module 9 Read more
Currently available on:
- 2. Dec 2019
- 1. Dec 2020
Promotion in the Nordics
Pharmaceutical marketing compliance in Sweden, Norway, Finland and Denmark Read more
Currently available on:
- 13. Nov 2019
Quality - Drug Substance and Drug Product
Module 6 Read more
Currently available on:
- 4. Nov 2019
- 18. Nov 2020
Risk Management from an ICH-GCP E6 (R2) perspective
Understand risk management principles and the links between study level risk management and the ... Read more
Sales Intelligence
Learn about the key theories used for analyzing markets and how to use market data Read more
Currently available on:
- 21. Apr 2020
Securing Market Uptake
Learn whom to talk to when, why and how Read more
Currently available on:
- 26. Feb 2020
The EU Regulatory Environment - Procedures and Applications
Module 2 Read more
Currently available on:
- 2. Sep 2020
The Pharmaceutical Law Frameworks in the EU
Module 1 Read more
Currently available on:
- 11. May 2020
The Regulatory Affairs Environment for Generic Products in the EU
Module 15 Read more
The Regulatory Affairs Environment in Japan
Module 4 Read more
Currently available on:
- 3. Nov 2020
The Regulatory Affairs Environment in the USA
Module 3 Read more
Currently available on:
- 8. Jun 2020
Understanding Pharma
Get the competences to start a successful career in the pharmaceutical industry Read more
Currently available on:
- 10. Dec 2019
- 3. Mar 2020
Using Evidence
Learn how to critically process and analyse medical scientific literature Read more
Currently available on:
- 2. Dec 2019
- 9. Jun 2020
Veterinary Pharmacovigilance
Module 8 Read more
Veterinary Regulatory Affairs in the EU
Module 14 Read more
Exams
Exam Adverse Drug Reactions by Body Systems
Exam Diploma in ICH-GCP Managed trials
Exam Global Regulatory Strategies
date: 24. Feb 2020
Exam Marketing Compliance
date: 26. Aug 2020
Exam Medical Devices - Drug/Device Combinations
Exam Non-clinical Development and Documentation
Exam Pharmacoepidemiology
date: 5. Nov 2019
Exam Pharmacovigilance Data in Application and Registration
date: 16. Dec 2019
Exam Pharmacovigilance Systems Master File
Exam Post-Marketing Surveillance
date: 9. Jan 2020
Exam Preclinical and Clinical Aspects of Pharmacovigilance
Exam Principles of Pharmacovigilance
Exam Product Life Cycle Activities
date: 7. Jan 2020
Exam The Pharmaceutical Law Frameworks in the EU
date: 11. Jun 2020
Exam The Regulatory Affair Environment in Japan
Exam The Regulatory Affairs Environment for Generic Products in The EU
Exam Veterinary Pharmacovigilance
Replacement of Certificate
date: 31. Dec 2019
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
Currently available on:
- 28. Jan 2020
Marketing compliance network 2019/2020
A network for individuals working with marketing compliance in a pharmaceutical company Read more
Currently available on:
- 23. Oct 2019
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:
- 12. Nov 2019
Hot Topic: Challenges for global Regulatory Strategies beyond the EU, US and Japan
Learn the most crucial regulatory issues when defining global regulatory strategies incorporating ... Read more
Currently available on:
- 28. Nov 2019
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