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  Comment développer votre compliance et votre efficience en tant qu’AQ?

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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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  Auditor/Lead Auditor – Läkemedel och medicinteknik

  €2 435,00 €2 140,00 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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  CGMP för kvalitetskontroll (QC) och analysarbete

  €665,00 €615,00 Add to cart
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  Cleaning validation of pharmaceutical process equipment

  €1 950,00 €1 750,00 Add to cart
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  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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  Decontamination process and validation

  €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
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  FDA Enforcement and Compliance Trends

  €350,00 Add to cart
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  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