Software that enables medical device companies to continuously analyze and improve the efficiency of operations through a single solution.
Read this article to learn where organizations are failing and what they need to do to achieve sustainable high performance in their processes.
Leading the transformation process to sustainable high performance
Read this article to learn how organizations can improve business processes in a highly effective way and without any frustration.
A blended approach to Business Process Improvement deployment
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 – Ce que vous devez savoir
Learn how organizations can improve business processes, deliver greater stakeholder value and stand out among the competition.
Connecting Processes to Business Value: What is End-to-End Process Architecture?
Tools and techniques to finding solutions, how to avoid common misuse of the process and how to use it for success in your organization.
Understanding Root Cause Analysis
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