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
Read this article to learn how to identify and asses vendor risks from an ERM perspective, avoiding surprises and helping the organization to achieve its goals.
Using an ERM Assessment Process to understand vendor risks
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
The EHS department can be housed in a wide variety of locations within an organization. What is its optimal placement?
The “Right Home” for Environment, Health and Safety
Watch this webinar and find out what changes in the new ISO 45001, key requirements, benefits and how you can start implementing the standard.
Replacing OHSAS 18001: What do you know about ISO 45001?
Watch this Webinar to learn how ISO 45001 can help your company to improve employee safety, reduce workplace risks and create better, safer working conditions.
Achieving Excellence in OH&S with ISO 45001
SE Supply is a supply management software that helps organizations automate warehouse and distribution operations.
Supply Management – SE Supply
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
The several factors that must be considered when determining the appropriate sample size for process validation.