How to transform life sciences industry landscape and achieve business excellence
Comment transformer le panorama de l’industrie des sciences de la vie et atteindre l’excellence en affaires
Read this eBook and learn about 8 cornerstones that help in overcoming obstacles on the journey to Industry 4.0.
Building a digital company: 8 cornerstones for success in Industry 4.0
Read this article and find out more on how a Document Control System may help companies to ensure regulatory compliance.
Why my electronic “Document Control System” may only be a “Document Management System”
Software that enables medical device companies to continuously analyze and improve the efficiency of operations through a single solution.
An overview of ISO 26000, its main clauses, links between ISO 26000 with other standards, benefits certification path and more.
ISO 26000 – Social Responsibility
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
Read this eBook and be better prepared to conduct a smooth transition of ISO 13485 at your organization.
ISO 13485:2016 – What you need to know
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?
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?
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