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 launches this fall
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-Headshot-Square

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

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.

Skærmbillede 2022-05-10 kl. 13.05.16

Stine Kristensen has more than 15 years of pharma industry experience working with IT Compliance, IT Implementation Projects, and System Administration. She has worked both as an external consultant and as internal staff for biotech, pharmaceutical and pharma-related device companies. Stine has worked as IT QA in operation and project phases for computerized systems and Validation Track Lead, as well as in GxP system/infrastructure operation and maintenance. She holds a CISA certification, a SAFe Scrum Master certification, and is trained as Lead auditor for internal and external audits.

Birgitte Circle

Birgitte Sloth holds 18 years of experience in the pharma industry and academia, working with Clinical Science and Global Trial Management (Phase I-III) both as Clinical Scientist, Global Trial Manager, Clinical Project Manager, and People Lead. As Pharma IT’s VP of Clinical Operations, she leads our team of expert Clinical Science & Trial Operations and Medical Writing Consultants. Birgitte has experience with planning, conduct and finalization of different trials with focus on early phase projects, and proof of concept trials in multiple different indications, and she is also experience with rare disease programs. She holds both a PhD and Postgraduate Diploma Degree in Pharmaceutical Medicine with a focus in Clinical Pharmacology.

 

Maria Iversen Circle

Maria Iversen has 13 years of experience as global study manager. She has in-depth experience in planning, running and managing international phase I-IV clinical studies in multiple indications from protocol development to finalization of the clinical study report and reporting of results. Maria has also worked as project manager, providing strategic input to implementation of EU Clinical Trial Regulation (CTR) as well as providing support setting up internal GCP processes. She holds a M.Sc. in pharmaceutical science and works as a Principal Consultant at Pharma IT.

Upcoming Pharma IT Academy Courses & Events

Good Manufacturing Practice (GMP) Basics
Danish: September 21-22, 2022
English: November 22-23, 2022

6500 DKK (ex moms)*

GAMP 5 & Computer System Validation (CSV) Basics
Danish: September 28-29, 2022
English: November 1-2, 2022

9995 DKK (ex moms)*

Good Clinical Practice (GCP) Basics

Danish: November 16, 2022
English: March 2, 2023

4995 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.

Unpacking ISPE’s New GAMP®5 Guide Second Edition with Sion Wyn
November 8th|2000 DKK (ex moms)*

Join us in-person this November for an afternoon in conversation with world-renowned computer system validation expert and editor of ISPE’s GAMP®5 Guide, Sion Wyn.

Program
16:00 Welcome, Coffee & Cake
16:30 Keynote by Sion Wyn
18:00 Q & A
18:30-20:00 Networking w/ Tapas & Wine

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.

Marika Rasmussen, Director of Education, Training, & Certification

The Pharma IT Academy launches this fall 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.

Upcoming Pharma IT Academy Courses

Good Manufacturing
Practice (GMP)
Danish: September 21-22, 2022
English: November 22-23, 2022
6500 DKK (ex moms)*

GAMP 5 & Computer System Validation (CSV)
Danish: September 28-29, 2022
English: November 1-2, 2022
9995 DKK (ex moms)*

Good Clinical Practice (GCP) Basic
Danish: November 16, 2022
English: March 2, 2023
4995 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.

Special Event: Unpacking ISPE’s New GAMP®5 Guide Second Edition with Sion Wyn

November 8 – 2000 DKK (ex moms)
Join us in-person for an afternoon in conversation with world-renowned computer system validation expert and editor of ISPE’s GAMP®5 Guide, Sion Wyn.

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?