24 item(s)
Cases
The tool allowed for the continuous improvement of processes, in addition to supporting the achievement of the certification by ONA and ISO 9001 certification
Santa Rita Hospital and Maternity automates processes and earns ONA hospital certification with a SoftExpert solution
Ebook
Read this eBook and learn how technology can contribute to meeting the resolution on GMP for medical devices.
GMP: How to implement them in the medical device industry
Ebook
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
White Paper
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
Webinar
Watch to this webinar and find out more on how a Document Control System may help companies to ensure regulatory compliance.
How to establish a Document Control System to ensure ISO and FDA compliance
Ebook
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
Ebook
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
White Paper
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”
Video
Software for the management of the healthcare sector, promoting the efficiency of the production process and using the best practices of the market.
Healthcare
Video
Software that enables medical device companies to continuously analyze and improve the efficiency of operations through a single solution.
Medical Devices
White Paper
Device Master Records and Medical Device files are FDA requirements. How do they compare?
Device Master Records and Medical Device Files – How Do They Compare?
White Paper
Managing third party audits is important in a regulated environment, to confirm that suppliers are providing the highest quality products and services.