In-company Courses
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Kursus i virksomheden
New
GDP
Ready for Inspection|company
Be Ready for Your Next Regulatory Inspection
Understand the requirements, roles and appropriate conduct before, during and after an inspection. Employees receive practical advice to help your com...
Understand the requirements, roles and appropriate conduct before, during and after an inspection. Employees receive practical advice to help your com...
Kursus i virksomheden
Nyt
GDP
Klar til inspektion|virksomhed
Bliv klar til næste myndighedsinspektion
Få styr på krav, roller og god adfærd før, under og efter en inspektion. Medarbejderne får konkrete råd, så I kan møde inspektøren roligt, fagligt og ...
Få styr på krav, roller og god adfærd før, under og efter en inspektion. Medarbejderne får konkrete råd, så I kan møde inspektøren roligt, fagligt og ...
Kursus i virksomheden
Nyt
GMP – kvalitetsstyring og compliance
Robuste SOP’er – din nøgle til compliance|virksomhed
Lær at skrive SOP'er, der er nemme at forstå og understøtter compliance
Skriv SOP’er, der bliver læst, forstået og fulgt.På kurset får medarbejderne fælles værktøjer til at gøre instruktioner mere tydelige, mere anvendelig...
Skriv SOP’er, der bliver læst, forstået og fulgt.På kurset får medarbejderne fælles værktøjer til at gøre instruktioner mere tydelige, mere anvendelig...
Kursus i virksomheden
New
GMP – kvalitetsstyring og compliance
Requirements for Production Facilities and Equipment in a Controlled Environment|company
Learn How Facilities and Equipment Support Product Quality
Employees gain insight into GMP requirements for facilities and equipment and an understanding of how facilities and equipment support quality, compli...
Employees gain insight into GMP requirements for facilities and equipment and an understanding of how facilities and equipment support quality, compli...
Kursus i virksomheden
Kort operatørkursus
Introduction to the Manufacture of Sterile Medicinal Products for Operators|company
Get New Operators Ready to Work in Your Sterile Manufacturing Environment
The course prepares new operators to work in accordance with GMP requirements in your organisation and gives them a clear understanding of the require...
The course prepares new operators to work in accordance with GMP requirements in your organisation and gives them a clear understanding of the require...
Kursus i virksomheden
GMP – kvalitetsstyring og compliance
Basic GMP for New Operators|company
Get New Operators Ready to Start in Your Pharmaceutical Manufacturing Environment
This course is a condensed two-day programme aimed at new operators in your organisation.It provides a basic understanding of GMP requirements and the...
This course is a condensed two-day programme aimed at new operators in your organisation.It provides a basic understanding of GMP requirements and the...
Kursus i virksomheden
GMP – kvalitetsstyring og compliance
Annex 1 – Aseptic Manufacturing|company
Understand the Requirements for Sterile Medicinal Products and Learn How to Apply Them in Your Organisation
Sterile medicinal products place extremely high demands on the environment, equipment, processes and behaviour.This company-focused course gives emplo...
Sterile medicinal products place extremely high demands on the environment, equipment, processes and behaviour.This company-focused course gives emplo...
Kursus i virksomheden
New
GMP – kvalitetsstyring og compliance
Robust SOPs – Your Key to Compliance|company
Learn how to write SOPs that are easy to understand and support compliance.
Write SOPs that are read, understood and followed.In this course, employees gain practical tools to make instructions clearer, more useful and easier ...
Write SOPs that are read, understood and followed.In this course, employees gain practical tools to make instructions clearer, more useful and easier ...
Kursus i virksomheden
New
GMP – kvalitetsstyring og compliance
The Effective Support Professionel|company
Strengthen Your Role in Collaboration with QA, Operations and Management
As a support professional, employees need to be able to act professionally and apply their professional expertise – even in challenging situations.
As a support professional, employees need to be able to act professionally and apply their professional expertise – even in challenging situations.
Kursus i virksomheden
New
GMP – kvalitetsstyring og compliance
GMP Documentation – Get It Right|company
Good Documentation Practices: Clear, Correct and Traceable
Documentation is a key element of GMP and essential for patient safety.It is rarely the major errors that cause problems. More often, it is the small ...
Documentation is a key element of GMP and essential for patient safety.It is rarely the major errors that cause problems. More often, it is the small ...
Kursus i virksomheden
New
GMP – kvalitetsstyring og compliance
GMP – from Regulatory Requirements to Everyday Practice|company
Understand Regulatory Requirements in Your Everyday Work
Do you understand why you do things the way you do?And do you know how much of a difference your individual contribution makes to the finished medicin...
Do you understand why you do things the way you do?And do you know how much of a difference your individual contribution makes to the finished medicin...
Kursus i virksomheden
New
GMP – kvalitetsstyring og compliance
Qualification and Validation – from Requirements to Testing|company
Get the Basics of Qualification and Validation
Gain an understanding of the requirements for qualification and validation when new equipment or processes are introduced in pharmaceutical manufactur...
Gain an understanding of the requirements for qualification and validation when new equipment or processes are introduced in pharmaceutical manufactur...
Kursus i virksomheden
New
GMP – kvalitetsstyring og compliance
Learn from Your Own Cases and Create a Shared Direction|company
Take part in a facilitated workshop where you set aside dedicated time to understand and learn from your own cases.
Do you have deviations, SOPs, audit findings, collaboration challenges or other production-related cases that would benefit from dedicated time togeth...
Do you have deviations, SOPs, audit findings, collaboration challenges or other production-related cases that would benefit from dedicated time togeth...
Kursus i virksomheden
New
GMP – kvalitetsstyring og compliance
From Compliance to a Culture of Quality|company
When Quality Becomes More Than Compliance
Learn how to translate GMP into everyday practice so that you not only comply with requirements, but also actively contribute to a strong quality cult...
Learn how to translate GMP into everyday practice so that you not only comply with requirements, but also actively contribute to a strong quality cult...
Kursus i virksomheden
GMP – kvalitetsstyring og compliance
Good Documentation Practice|company
Effective GMP Documentation in Your Organisation
Gain a clear understanding of regulatory requirements for proper GMP documentation and learn how to correctly complete and make corrections to batch d...
Gain a clear understanding of regulatory requirements for proper GMP documentation and learn how to correctly complete and make corrections to batch d...
Kursus i virksomheden
Nyt
GMP – kvalitetsstyring og compliance
Fra compliance til kvalitetskultur|virksomhed
Når kvalitet bliver mere end compliance
Lær at omsætte GMP, så I ikke kun følger kravene, men også bidrager aktivt til en stærk kvalitetskultur, der styrker både patientsikkerhed, data og sa...
Lær at omsætte GMP, så I ikke kun følger kravene, men også bidrager aktivt til en stærk kvalitetskultur, der styrker både patientsikkerhed, data og sa...
Kursus i virksomheden
Nyt
GMP – kvalitetsstyring og compliance
Lær af egne cases og få fælles retning|virksomhed
Få en faciliteret workshop, hvor I afsætter fælles tid til at forstå og lære af egne cases
Har I afvigelser, SOP’er, auditfindings, samarbejdsudfordringer eller andre produktionscases, som kalder på tid sammen til at opnå indsigt og vigtig l...
Har I afvigelser, SOP’er, auditfindings, samarbejdsudfordringer eller andre produktionscases, som kalder på tid sammen til at opnå indsigt og vigtig l...
Kursus i virksomheden
Nyt
GMP – kvalitetsstyring og compliance
Kvalificering og validering – fra krav til test|virksomhed
Opnå ”the basics” indenfor kvalificering og validering
Få styr på krav til kvalificering og validering, når nyt udstyr eller nye processer skal bruges i lægemiddelfremstilling – og lær at sikre sporbarhed ...
Få styr på krav til kvalificering og validering, når nyt udstyr eller nye processer skal bruges i lægemiddelfremstilling – og lær at sikre sporbarhed ...
Kursus i virksomheden
Nyt
GMP – kvalitetsstyring og compliance
GMP – fra lovkrav til hverdag|virksomhed
Forstå lovkravene i din hverdag
Forstår I, hvorfor I gør, som I gør?Og ved I, hvor stor en forskel den enkeltes indsats gør for det færdige lægemiddel?
Forstår I, hvorfor I gør, som I gør?Og ved I, hvor stor en forskel den enkeltes indsats gør for det færdige lægemiddel?
Kursus i virksomheden
Nyt
GMP – kvalitetsstyring og compliance
Krav til produktionsfaciliteter og udstyr i et kontrolleret miljø|virksomhed
Lær, hvordan lokaler og udstyr understøtter produktkvalitet
Medarbejderne får indsigt i GMP-kravene til lokaler og udstyr og forståelse for, hvordan faciliteter og udstyr understøtter kvalitet, compliance og pa...
Medarbejderne får indsigt i GMP-kravene til lokaler og udstyr og forståelse for, hvordan faciliteter og udstyr understøtter kvalitet, compliance og pa...
Kursus i virksomheden
Nyt
GMP – kvalitetsstyring og compliance
Styr på GMP-dokumentation|virksomhed
God dokumentationspraksis: Klar, korrekt og sporbar
Dokumentation er et nøgleelement i GMP og afgørende for patientsikkerheden.Det er sjældent de store fejl, der giver problemer. Ofte er det de små deta...
Dokumentation er et nøgleelement i GMP og afgørende for patientsikkerheden.Det er sjældent de store fejl, der giver problemer. Ofte er det de små deta...
Kursus i virksomheden
Nyt
GMP – kvalitetsstyring og compliance
Effektive CAPA’er|virksomhed
Lær at skabe CAPA'er, der virker i praksis
Lær værdien af CAPA, hvordan de kan fastlægges, implementeres og evalueres som en naturlig del af en kontinuerlig forbedringsproces.
Lær værdien af CAPA, hvordan de kan fastlægges, implementeres og evalueres som en naturlig del af en kontinuerlig forbedringsproces.
Kursus i virksomheden
Nyt
GMP – kvalitetsstyring og compliance
Root Cause Analysis|virksomhed
Få systematisk tilgang til problemløsning
Lær at arbejde systematisk med Root Cause Analysis i en GMP-kontekst, og få konkrete værktøjer til at identificere årsager til problemer og sikre løsn...
Lær at arbejde systematisk med Root Cause Analysis i en GMP-kontekst, og få konkrete værktøjer til at identificere årsager til problemer og sikre løsn...
Kursus i virksomheden
Nyt
GMP – kvalitetsstyring og compliance
Den stærke supporter|virksomhed
Stå stærkere i samarbejdet med QA, drift og ledelse
Som supporter skal medarbejdere kunne agere fagligt og professionelt – også i pressede situationer.
Som supporter skal medarbejdere kunne agere fagligt og professionelt – også i pressede situationer.
Kursus i virksomheden
GMP – kvalitetsstyring og compliance
Annex 1 – aseptisk produktion|virksomhed
Forstå kravene til sterile lægemidler og lær at omsætte dem til praksis i jeres virksomhed
Sterile lægemidler stiller ekstremt høje krav til miljø, udstyr, processer og adfærd. På dette virksomhedsrettede kursus får medarbejderne overblik ov...
Sterile lægemidler stiller ekstremt høje krav til miljø, udstyr, processer og adfærd. På dette virksomhedsrettede kursus får medarbejderne overblik ov...
Kursus i virksomheden
GMP – kvalitetsstyring og compliance
Grundlæggende GMP for nye operatører|virksomhed
Bliv hurtigt klar til start som operatør i jeres lægemiddelproduktion
Kurset er et komprimeret to-dages forløb målrettet nye operatører i jeres organisation. Det giver en grundlæggende forståelse for GMP-reglerne og de k...
Kurset er et komprimeret to-dages forløb målrettet nye operatører i jeres organisation. Det giver en grundlæggende forståelse for GMP-reglerne og de k...
Kursus i virksomheden
GMP – kvalitetsstyring og compliance
God dokumentationspraksis|virksomhed
Effektiv GMP-dokumentation i jeres organisation
Få en klar forståelse af myndighedernes krav til korrekt GMP-dokumentation og lær, hvordan batchdokumentation udfyldes og korrigeres korrekt i en GMP-...
Få en klar forståelse af myndighedernes krav til korrekt GMP-dokumentation og lær, hvordan batchdokumentation udfyldes og korrigeres korrekt i en GMP-...
Kursus i virksomheden
Kort operatørkursus
Introduktion til fremstilling af sterile lægemidler til operatører|virksomhed
Bliv klar til start som operatør i jeres produktion af sterile lægemidler
Kurset gør nye operatører klar til at arbejde efter GMP-reglerne i jeres organisation og giver dem en klar forståelse af de krav, der gælder i en ster...
Kurset gør nye operatører klar til at arbejde efter GMP-reglerne i jeres organisation og giver dem en klar forståelse af de krav, der gælder i en ster...
Kursus i virksomheden
GMP – kvalitetsstyring og compliance
Annual GMP|company
Updating is key to success in your life science organisation
Get documentation of maintained GMP knowledge, insight into current GMP trends, and the opportunity to exchange experience within your organisation.
Get documentation of maintained GMP knowledge, insight into current GMP trends, and the opportunity to exchange experience within your organisation.
Kursus i virksomheden
GMP – kvalitetsstyring og compliance
Root Cause Analysis and CAPA|company
Become an expert in handling problems and improving quality within your organisation
Gain insight into the techniques behind Root Cause Analysis (RCA) and learn how your organisation can plan and implement effective Corrective and Prev...
Gain insight into the techniques behind Root Cause Analysis (RCA) and learn how your organisation can plan and implement effective Corrective and Prev...
Kursus i virksomheden
GMP – kvalitetsstyring og compliance
Årlig GMP|virksomhed
Opdatering er nøglen til succes i jeres life science-organisation
Få dokumentation for vedligeholdt GMP-viden, indsigt i aktuelle GMP-trends og mulighed for erfaringsudveksling på tværs af jeres organisation.
Få dokumentation for vedligeholdt GMP-viden, indsigt i aktuelle GMP-trends og mulighed for erfaringsudveksling på tværs af jeres organisation.
Kursus i virksomheden
GMP – kvalitetsstyring og compliance
Root Cause Analysis og CAPA|virksomhed
Bliv ekspert i problemhåndtering og kvalitetsforbedring i jeres organisation
Få indsigt i teknikkerne bag Root Cause Analysis (RCA) og lær, hvordan jeres virksomhed kan planlægge og implementere effektive korrigerende og foreby...
Få indsigt i teknikkerne bag Root Cause Analysis (RCA) og lær, hvordan jeres virksomhed kan planlægge og implementere effektive korrigerende og foreby...
Kursus i virksomheden
GMP – kvalitetsstyring og compliance
Basic GMP|company
Understand GMP and learn how your organisation works with GMP in practice
Get a solid introduction to GMP and the EU’s regulations for pharmaceutical manufacturing and build a shared understanding across your team of the req...
Get a solid introduction to GMP and the EU’s regulations for pharmaceutical manufacturing and build a shared understanding across your team of the req...
Kursus i virksomheden
GMP – kvalitetsstyring og compliance
Grundlæggende GMP|virksomhed
Forstå GMP og lær hvordan jeres organisation arbejder med GMP i praksis
Få en solid introduktion til GMP og EU’s regler for fremstilling af lægemidler, og opbyg en fælles forståelse i jeres team for de krav, det ansvar og ...
Få en solid introduktion til GMP og EU’s regler for fremstilling af lægemidler, og opbyg en fælles forståelse i jeres team for de krav, det ansvar og ...
Benefits of an in-house training course
- Compliance – everyone hears the same message and gains a shared foundation for ensuring compliance with legal requirements.
- Effective – a shared starting point provides the foundation for implementing effective improvements.
- Sustainable – the instructor travels, rather than all the students.
- Cost-effective – much cheaper than sending 15 employees to a standard training course.
- Certification – all employees receive a certificate of completion.
- Quality – the instructor has experience in the life sciences and a background in education.
- The course is based on a well-defined curriculum—participants themselves determine its relevance through questions, discussion, and their own experiences.
- You’ll develop a shared understanding and a common language.
Here's how it works
- Select a course, time, and location (see below) and send us a message using this form.
- We will find an instructor with experience in this field.
- Perhaps we can discuss how to align your schedules with ours.
- We will send you a contract, and once you have approved it, the course will be booked.
- You can provide the venue and audiovisual equipment, or you can ask us to make a reservation at Pharmakon.
- We teach.
- You will receive course certificates for the courses you have completed.
Course Formats
Courses are available in various formats:
- Half-day courses (e.g., 9 a.m.–12 p.m. or 1 p.m.–4 p.m.). You may choose to combine two half-day courses or combine the day with your own activities in the department.
- 1-day courses (9 a.m.–4 p.m.). We’ve put together the program to give you the opportunity to ensure implementation as the course progresses.
- Two-day courses are particularly well-suited for a department that needs both knowledge and an understanding of the unique aspects of drug manufacturing.
Location
In-house training courses take place—as the name suggests—at the company’s premises.
Please note that you’ll get the most out of the course when:
- There are chairs and tables for everyone.
- Everyone can see the instructor and the presentation.
- There is room for group discussions.
- Refreshments will be provided during breaks and for lunch.
If you don’t have suitable facilities, we’d be happy to come to a training location of your choice.
The course can also be held at Pharmakon, where we have excellent facilities and catering—in which case we will handle the room reservations. If the course is held at Pharmakon, you will receive a 10% discount on room rental fees and any accommodation costs.
Finally, the course can be taken online—please feel free to ask us if you’re interested.
How much does an in-house training course cost?
The prices include course materials for participants and the instructor’s travel expenses; in other words, the price you see here is the total amount your company will pay.
½ day with 1 instructor and up to 24 participants
25,000 DKK, excluding VAT (2026)
25,700 DKK, excluding VAT (2027)
1 day with 1 instructor and up to 24 participants
45,300 DKK, excluding VAT (2026)
46,600 DKK, excluding VAT (2027)
2 days with 1 instructor and up to 24 participants
80,300 DKK, excluding VAT (2026)
82,550 DKK, excluding VAT (2027)
Frequently Asked Questions
Is the course tailored to our company?
No—it’s a standard course. We use a dialogue-based approach and draw on the participants’ own experiences and challenges, allowing you to relate the content to your daily work.
How many participants can there be?
Typically up to 24 people. If there are more of you, please contact us to discuss the details.
Is it possible to combine multiple topics?
No, you can only take one course at a time—but you’re welcome to book multiple courses over time.
Can the course be held in English?
Yes, all courses at the company can be held in either Danish or English—the choice is yours.
Who chooses corporate training courses?
- Production and quality departments seeking a shared understanding.
- Companies with many new employees.
- Teams that need a refresher on specific topics.
- Organizations that want to keep learning closely tied to real-world practice.
Get proof of your skills
An in-house training course concludes with a certificate of completion, which serves as proof that the individual employee has participated in the course.
Want to know more?
Elizabeth Ruelykke
Course Coordinator
+45 48 20 62 64 erk@pharmakon.dk