Real-world compliance training led by practicing industry experts
Forget boring, slide-deck, theory-only learning.
Come learn from the best in the business.
Real-world compliance training led by practicing industry experts
Forget boring, slide-deck, theory-only learning. Come learn from the best in the business.
The Pharma IT Academy
with trainings in GMP, CSV, and more
Learn directly from practicing compliance experts with decades of industry experience
Our instructors are veteran consultants who work with course concepts on a daily basis. You’ll learn from their real world experience, knowledge, and expertise.
Experience modern teaching methodologies and the most
up-to-date curriculum
No more boring, theory-only, slide deck learning. Our instructors use an engaging, interactive, and case-based approach aligned with the latest, and upcoming, authority regulations.
Gain access to Pharma IT’s expert consultants beyond your time in the classroom
Pharma IT Academy Alumni gain access to the Pharma IT Network! So you can ask our experts any follow up questions you have once you start using course skills in the field.
Meet the Pharma IT Academy's Expert Instructors
Dorte Juul holds more than 15 years’ experience within the IT compliance area, working in both the pharmaceutical industry and food ingredients sector, and is highly specialized in GxP. She has performed in leading roles, such as Validation Track Lead on projects, as well Service and Release Manager on production systems. Dorte holds a master’s degree in International Business. She has SAFe Agilist, SAFe Scrum Master and CISA certifications as well as an ITIL Foundation Certification and certifications as Computer Validation Manager and Lead Auditor.
Torben Elhauge has more than 25 years’ experience in GMP regulated areas and holds a master’s degree in chemical engineering. He has broad experience within all parts of the CMC area – from development over validation and registration to GMP release of products. He has in-depth knowledge of the regulatory landscape and worked at the Danish Medicines Agency for more than 6 years. He has also worked within the QA area, conducting GMP training and audits. He has extensive training experience lecturing for the MIND at KU, Pharmakon, Lægemiddelstyrelsen, as well as internal GMP related courses for several Pharma IT customers.
Trine Stougaard holds 18+ years of experience with the operational aspects of planning and conducting global clinical phase II-IV trials and non-interventional studies (from idea to publications incl. planning and conduct of Global Expert Panels). Extensive experience with outsourced clinical trials (from contracting to publications), CRO collaboration including CRO oversight, project management and stakeholder management.
Upcoming Pharma IT Academy Courses & Events
EU Regulatory Affairs 2025: Latest Updates and Expert Insights Event
English: February 25, 2025
2000 DKK (ex moms)*
Good Manufacturing Practice (GMP) Basics
English: January 28-29, 2025
10995 DKK (ex moms)*
Computer System Validation (CSV) & GAMP5 Basics
English: February 26-27, 2025
11995 DKK (ex moms)*
Clinical Development and Applied Good Clinical Practice (GCP) Course
English: February 4, 2025
7995 DKK (ex moms)*
Are you currently unemployed and wish to sign up to our courses, then we have gathered some information.
Upcoming Pharma IT Academy Master Class
Exciting News!
We are now able to offer a new Master Class! This is for you who already have the basic GxP knowledge and wants to further develop your competencies.
Master Class in Extractables and Leachables
Danish: March 28th, 2023
English: March 29th, 2023
7500 DKK (ex moms)*
*For inquiries regarding group rates and pricing for on-site training, please contact the Pharma IT Academy team by using the contact button below.
Lifelong learning is essential to your professional development in the life sciences — an industry dedicated to developing lifesaving medicinal products and devices for millions of people around the world
That’s why we have launched the Pharma IT Academy — to improve the standards of compliance training and empower you with the skills you need to ensure patient safety.
We know that learning through engaging teaching methods helps participants retain more information and improves their ability to utilize course concepts long after they return back to their workplace.
So, we’ve moved away from the one-way, slide-deck, and theory-only teaching approach, and incorporated a broad variety of interactive learning methods and innovative learning environments.
On top of that, your Pharma IT Academy course registration includes a 1-free year membership to the Pharma IT Network — where you’ll have access to our expert instructors beyond the classroom to give you the best start applying the course concepts in your daily work.
The Pharma IT Academy aims to provide a vibrant network of driven life science professionals that inspires, and high-end quality courses that stand out amongst the crowd. We hope to fuel your learning journey, whether you are just breaking into the life sciences industry or are looking to level up your skills for the next step in your career.
That’s how we want to make a difference.
Naomi Jade Kellogg, Education, Training, & Certification Lead
The Pharma IT Academy is your one-stop GxP training shop
Learn directly from practicing compliance experts with decades of industry experience
Our instructors are veteran consultants who work with course concepts on a daily basis. You’ll learn from their real world experience, knowledge, and expertise.
up-to-date curriculum
No more boring, theory-only, slide deck learning. Our instructors use an engaging, interactive, and case-based approach aligned with the latest, and upcoming, authority regulations.
Pharma IT Academy Alumni gain access to the Pharma IT Network! So you can ask our experts any follow up questions you have once you start using course skills in the field.
Upcoming Pharma IT Academy Courses
EU Regulatory Affairs 2025: Latest Updates and Expert Insights Event
English: February 25, 2025
2000 DKK (ex moms)*
Good Manufacturing
Practice (GMP) Basics
English: January 28 -29, 2025
10995 DKK (ex moms)*
GAMP 5 & Computer System Validation (CSV)
English: February 26-27, 2025
11995 DKK (ex moms)*
Clinical Development and Applied Good Clinical Practice (GCP) Course
English: February 4, 2025
7995 DKK (ex moms)*
GDPR & Data Privacy in Life Science
English: June 24th, 2025
6500 DKK (ex moms)*
NIS2 & Cybersecurity in Life Science
English: June 25th, 2025
6500 DKK (ex moms)*
*For inquiries regarding group rates and pricing for on-site training, please contact the Pharma IT Academy team by using the contact button below.
Pharma IT can provide tailored services and solutions for firms of all sizes
You can find our consultants working with customers of all sizes – from Danish pharma giants to budding biotech and medical device start-ups. Whether you are looking for a large-scale and long-term solution, or short-term assistance, Pharma IT can help.
Looking for a course that isn't listed?
Interested in a course held in English? Have other questions?
Looking for a course that isn't listed?
Interested in a course held in English? Have other questions?