Discover the key factors that high-tech companies need to address to achieve operational excellence.
How to achieve excellence in the operations of high-tech companies
Read this eBook to learn how your company can go farther and achieve its process automation objectives with BPM and RPA.
BPM + RPA: Taking process automation to another level
Read this eBook to find out the nine pillars to help medical device companies overcome barriers to excellence.
How to overcome challenges and boost results in the medical devices industry
How to choose the right suppliers, service providers and sub-tier suppliers, and how to monitor them to ensure FDA compliance.
Managing your Medical Device suppliers – Tips for ensuring they are truly FDA compliant
Lisez ce livre électronique et découvrez quelques stratégies qui vous aideront à passer du papier au format numérique en accélérantles processus dans votreentreprise.
Guide complet pour abolir l’utilisation du papier
Software that enables medical device companies to continuously analyze and improve the efficiency of operations through a single solution.
Certaines activités de base, ordonnées de manière logique, visent à promouvoir des directives simples mais efficaces pour un programme de gestion EHS.
Comment améliorer la gestion de la santé, de la sécurité et de l’environnement – SSMA
In this white paper, PECB discusses the main clauses of ISO 27001, its links with other standards and guidelines and more.
ISO 27001 – Information Technology Security Management
Watch this webinar to learn how an Integrated Management System can cut red tape and boost productivity at your business.
Enhancing regulatory compliance through the integrated approach
A webinar that shows a practical example of how to model and automate a business process, from start to finish, in less than 30 minutes.
How to model and automate a process in less than 30 minutes
SE Storeroom is a software solution that focuses on warehouse, stock and inventory management.
Storeroom Management – SE Storeroom
The several factors that must be considered when determining the appropriate sample size for process validation.