Change is occurring so rapidly with new regulations, laws, and customer demands that life science companies can no longer manage key documents and specifications in disparate systems. Improve the quality of your products, reduce development time, and increase cost savings by digitizing spec data into one system.Get Started
This all starts with digitization of your specification data.
Increase your operational efficiency by including your suppliers when you need them throughout your product lifecycle from ideation to recycling & reuse.
The Specright Specification Data Management platform is compliant with FDA 21 CFR Part 11. This regulation requires verification of all electronic documents and signatures being used in place of physical documentation for regulated purposes.
All our Specright services are also SOC2 compliant from security, confidentiality, and availability trust perspectives.
Specright allows companies to develop new products and versions faster by providing a central location for NPI activities and related data.
Go beyond tracking and managing your sustainability metrics - know the environmental impact of your products and packaging before they go to market.
One of the world's largest global medical device producers chose Specright to digitize packaging data and increase collaboration across their supply chain.
Learn how this company reduced project lead time from 40 weeks to 8 weeks and has 100% confidence that their data is accurate and complete.
Learn more about the value Specright can bring to your business from these resources.Specsights