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
Read this eBook to find out the eight pillars to help life sciences companies overcome barriers to excellence.
How to achieve Operational Excellence in the Life Sciences Industry
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.
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