Primary packaging materials for medicinal products - Particular requirements for the application of ISO 9001:2015, with reference to good manufacturing practice (GMP) - Amendment 1: Climate action changes (ISO 15378:2017/Amd 1:2024); German version EN ISO 15378:2017/A1:2024
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Medical device software - Medical SPICE - Recommendations for software development
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Primary packaging materials for medicinal products. Particular requirements for the application of ISO 9001:2015, with reference to good manufacturing practice (GMP)
€421.00
Medical electrical equipment Particular requirements for the basic safety and essential performance of photodynamic therapy diagnosis
€329.00
Medical electrical equipment Particular requirements for basic safety and essential performance of medical robots rehabilitation, assessment, compensation or alleviation
Technology enabled care. Assessment of user needs and risks, system design, installation and maintenance. Code of practice
Primary packaging materials for medicinal products - Particular requirements for the application of ISO 9001:2015, with reference to good manufacturing practice (GMP) - Amendment 1: Climate action changes (ISO 15378:2017/Amd 1:2024)
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Articles d'emballage primaire pour médicaments - Exigences particulières pour l'application de l'ISO 9001:2015 prenant en considération les Bonnes Pratiques de Fabrication (BPF) - Amendement 1 : Actions relatives aux changements climatiquesAutomatic translation from French : Primary packaging items for medicinal products - Particular requirements for the application of ISO 9001:2015 taking into account Good Manufacturing Practices (GMP) - Amendment 1: Actions relating to climate change
Évaluation biologique des dispositifs médicaux - Partie 17 : Appréciation du risque toxicologique des constituants des dispositifs médicaux - Amendement 1
Systems for evacuation of plume generated by medical devices (ISO 16571:2024); German version EN ISO 16571:2024
€140.00
Évaluation biologique des dispositifs médicaux - Partie 1 : Exigences et principes généraux pour l'évaluation de la sécurité biologique au sein d'un processus de gestion des risques
Évaluation biologique des dispositifs médicaux - Partie 6 : essais concernant les effets locaux après implantation
€146.00
Évaluation biologique des dispositifs médicaux - Partie 7 : Résidus de stérilisation à l'oxyde d'éthylène
€205.00
BS EN IEC 80601-2-31 Medical electrical equipment Part 2-31: Particular requirements for the basic safety and essential performance of external cardiac pacemakers with internal power source
€24.00
