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Key2Compliance® solves all your training needs in terms of regulatory requirements, GMP, GXP and quality systems. Knowledge of these requirements is an important key to developing, manufacturing and distributing safe and effective drugs and medical devices. Training from Key2Compliance® makes the knowledge easily accessible, applicable and makes it clear how the regulatory requirements affect your business.

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Cleaning validation of pharmaceutical process equipment – Course

Learn details for all part of the global cleaning validation strategy in pharmaceutical activities. CGMP expectations, technical and regulatory updates.
Nov 3
- Nov 5, 2026
Copenhagen & Kolding, Denmark
Cleanrooms and cleaning, Sterile products, Validation and Qualification

Auditor / Lead Auditor Course – Pharmaceuticals and Medical Devices

This tailor made training gives you the tools and skills required as Auditor or Lead Auditor in the Pharmaceutical and Medical Device industry.
Nov 9
- Nov 11, 2026
Copenhagen, Denmark
Auditing/Inspection

MDSAP – a global audit approach – Course

Learn how to plan perform and report internal MDSAP audits as well as best practice and tools how to be prepared to undergo or perform MDSAP audits.
Nov 24
- Nov 25, 2026
Copenhagen, Denmark
Auditing/Inspection, Quality management and QA

Validation and qualification – Course

Get in-depth knowledge of regulatory requirements regarding validation and qualification and their application in the pharmaceutical industry.

Nov 25
- Nov 26, 2026
Copenhagen, Denmark
Validation and Qualification

Course in Quality Risk Management and Root Cause Investigations

An overview of QRM and RCI and the respective regulatory expectations. Common tools and methods for the Pharma and Medical Device industry.
Dec 1
- Dec 3, 2026
Copenhagen, Denmark
QRM, Risk

Advanced Training in Biological Evaluation of Medical Devices

Learn how and when a biological evaluation, according to ISO 10993-1, should be performed. Understand the evaluation requirements and avoid common pitfalls!
Dec 8
- Dec 9, 2026
Mölndal-Gothenburg, Sweden
Biocompatibility

Cleaning validation of pharmaceutical process equipment – Course

Learn details for all part of the global cleaning validation strategy in pharmaceutical activities. CGMP expectations, technical and regulatory updates.
Mar 16
- Mar 18, 2027
Copenhagen & Kolding, Denmark
Cleanrooms and cleaning, Sterile products, Validation and Qualification

GMP-krav på datoriserade system – Kurs

Utbildning om de FDA och EU-regler och tolkningar som berör datoriserade och automatiserade system vid läkemedelstillverkning: 21 CFR 11 och EU GMP Annex 11
Apr 7
- Apr 8, 2027
Stockholm, Sweden
Computers/Software, GMP

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