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ISO13485:2016 – from an auditing perspective
€1 050,00€950,00 Add to cart -
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Auditor / Lead Auditor – Pharmaceuticals and Medical Devices
€2 550,00€2 250,00 Add to cart -
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CAPA and root cause analysis, tools for an effective CAPA process
€1 050,00€950,00 Add to cart -
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Cleaning validation of pharmaceutical process equipment
€1 950,00€1 750,00 Add to cart -
Clinical Evaluation for Medical Devices
€950,00 Add to cart -
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Contamination Control Strategy
€1 050,00€950,00 Add to cart -
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Design Controls for Medical Devices
€1 950,00€1 750,00 Add to cart -
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Effective root cause investigation for the Life Sciences
€1 950,00€1 750,00 Add to cart -
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EU Annex 1 – Manufacture of Sterile Medicinal Products
€1 950,00€1 750,00 Add to cart -
EU GMP Annex 1 – Highlight of the new industry requirements
€350,00 Add to cart -
FMEA Without Tears
€250,00 Add to cart -
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GMP Compliance and Auditing for Sterile Pharmaceuticals
€2 550,00€2 250,00 Add to cart -
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GMP-krav på datoriserade system
€1 330,00€1 230,00 Add to cart -
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Grundlæggende om GMP
€630,00€580,00 Add to cart -
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IVDR in a nutshell – the roadmap to CE-certification
€1 050,00€950,00 Add to cart -
La validation à l’heure du QbD…
€250,00 Add to cart
