EU
Showing 1–16 of 18 results
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ISO13485:2016 – from an auditing perspective
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CAPA and root cause analysis, tools for an effective CAPA process
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Clinical Evaluation for Medical Devices
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EU Annex 1 – Manufacture of Sterile Medicinal Products
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IVDR in a nutshell – the roadmap to CE-certification
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MDR Audit Readiness
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QA/RA Leader Medical Devices
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Risk Management according to ISO 14971:2019
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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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IVDR Readiness – prepare for the changes in the new IVDR
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