Lisez cet eBook et soyez mieux préparé pour effectuer une transition en douceur d'ISO 13485 dans votre organisation.
ISO 13485:2016 – Ce que vous devez savoir
How to select and manage external providers (processes, products and services) taking into account performance and risk-based thinking.
How to control externally provided processes, products and services
Tools and techniques to finding solutions, how to avoid common misuse of the process and how to use it for success in your organization.
Understanding Root Cause Analysis
The several factors that must be considered when determining the appropriate sample size for process validation.
Process Validation: How many sample sizes do I need?
SoftExpert PLM is an affordable, easy-to-use, and web-based software that allows companies to manage the entire lifecycle of a product.
Product Lifecycle Management – PLM
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SoftExpert Excellence Suite – SE Suite
The importance of the "risk based approach" for the correct performance and adequate safety of medical devices.
How will ISO 13485:2016 impact your relationship with suppliers?
Le modèle d’excellence en gestion et son utilisation systématique des pratiques et des outils clés.
7 Outils capital pour Excellence en Affaires
The key clauses of ISO 13485 and the business benefits of quality management in the medical devices industry.
ISO 13485 – Medical devices quality management systems
An overview on the transition process between the ISO/TS 16949 to IATF 16949.
Managing the transition from ISO/TS 16949 to IATF 16949
The differences among product line strategies, business strategies and corporate strategies.