Kurser: Pharma og medico

Få en grundlæggende forståelse af GMP, essentielle regler for lægemiddelfremstilling, og lær hvordan du sikrer høj produktkvalitet.

Gain a solid understanding of GMP and learn the key principles and their practical application in pharmaceutical manufacturing.

Learn the Usability Engineering process for medical devices and meet the requirements of ISO/IEC 62366-1:2015 and FDA guidelines.

Learn essential EU MDR, FDA and ISO 13485 compliance for medical devices across the full product lifecycle.

Vil du udvikle medicinsk udstyr, der er sikkert, effektivt, pålideligt og i overensstemmelse med de relevante standarder og regulativer?

Introduction to regulatory affairs in pharma: EU frameworks, documentation requirements, regulatory strategy and life cycle management.

Gain hands-on AI experience for Life Science manufacturing. Learn implementation, compliance and applications in pharma and medtech.

Gain hands-on knowledge of ISO 13485 and ensure your medical devices meet international standards.

Strengthen your understanding of Good Automated Manufacturing Practice (GAMP5)

Optimize the quality and efficiency during development of computerized systems with the GAMP5 AI Accelerated course.

Lær hvordan du får succes med din digitale rejse i et GMP reguleret miljø.

Få overblik over de mest lovende sundhedsteknologier – fra genterapi og RNA til stamceller, AI og præcisionsmedicin.

Få overblik over og forståelse for, hvordan klinisk udvikling af lægemidler foregår.

Learn to apply Quality Risk Management in life science – from ICH Q9 principles to practical risk assessment.