EU
Showing 1–16 of 19 results
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ISO13485:2016 – from an auditing perspective
€ 950 Add to cart -
IVDR in a nutshell – Technical Documentation
€ 490 Add to cart -
CAPA and root cause analysis, tools for an effective CAPA process
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Clinical Evaluation for Medical Devices
€ 950 Add to cart -
Sale!
EU Annex 1 – Manufacture of Sterile Medicinal Products
€ 1 750 Add to cart -
IVDR in a nutshell – the Quality Management System
€ 490 Add to cart -
MDR Audit Readiness
€ 620 Add to cart -
Sale!
QA/RA Leader Medical Devices
€ 2 250 Add to cart -
Risk Management according to ISO 14971:2019
€ 950 Add to cart -
The application of Good Distribution Practice (GDP) for the Responsible Person handling Pharmaceuticals
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Understand MDSAP Audit approach
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Det nya regelverket IVDR – är ditt företag redo?
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EN ISO14971:2019 – Risk management – in relation to MDR and ISO13485
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Ensure access to the Chinese market
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Equipment Management in the Pharmaceutical Supply Chain
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Grunnkurs i risikostyring (Risk management)
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