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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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Auditor / Lead Auditor – 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.
Oct 21
- Oct 23, 2025
Copenhagen, Denmark
Auditing/Inspection

Cleaning validation of pharmaceutical process equipment

Learn details for all part of the global cleaning validation strategy in pharmaceutical activities. CGMP expectations, technical and regulatory updates.
Nov 5
- Nov 7, 2025
Copenhagen & Kolding, Denmark
Cleanrooms and cleaning, Sterile products, Validation and Qualification

Alfa Laval Live Cleaning-in-Place Experience & Site Tour

Experience Cleaning-in-Place (CIP) technology in action, incl. sustainability-focused cleaning processes, real-life trials, with experts in cleaning validation.
Nov 7
Kolding, Denmark
cleaning in place, Sterilization

Medical Device Supplier Control and Outsourcing

Get tools and examples of best practice and learn how use the ‘Plan – Do – Check - Act approach’ to control and verify the performance of your suppliers.
Nov 19
- Nov 20, 2025
Copenhagen, Denmark
Quality management and QA

Design, Development and Regulatory Compliance for Medical Devices and SaMD

Learn how to apply design controls to ensure regulatory compliance for both hardware and software medical devices using agile development principles. This course covers ISO 13485, IEC 62304, EU MDR, FDA, risk management, SaMD, AI, and cloud-based technologies.
Nov 25
- Nov 26, 2025
Copenhagen, Denmark
ISO13485, IVDR, MDR, Regulatory Compliance

GMP Master Class (Svensk version)

Lär dig att förstå, navigera, tolka och tillämpa GMP enligt krav i både EU och USA, samt ICHs guidelines för kvalitetssystem och kvalitetsriskhantering.
Jan 20
- Jan 21, 2026
Stockholm, Sweden
Quality management and QA

Medical Device Quality Management Systems Training

Learn the key requirements of a quality management system in compliance with EU and US Medical Device regulations and how to implement them in your quality system.
Jan 28
- Jan 29, 2026
Copenhagen, Denmark
Quality management and QA

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