Regulatory agencies are now willing to accept paperless records but many producers in the food & beverage, pharmaceutical and biotech industries haven’t yet converted or even planned to transition to paperless solutions.
Robust record keeping is at the heart of FDA 21 CFR Part 11 compliance and while the regulation itself does not require users to maintain records electronically, the processing of data electronically has many advantages:
Define Instruments Cloud-based IIoT solutions provide a cost-effective way to store and harness your data digitally while complying with the FDA’s criteria.
Collect operational data from every machine for deeper insights into the workings of your business
Identify dead spots, inefficiencies, and untapped opportunities in your value chain
With data insights you can achieve greater productivity, planning and growth.
Cloud-based IIoT data recording is now more economic and more flexible than paper record keeping, and the network infrastructure required for data storage is significantly more accessible.
Additionally, compliance requirements such as restricted access for differing pay grades, password protection, digital signatures and data backups are all now easily available within Define’s IIoT solution.
It’s time to do away with your ageing paper system and upgrade to a modern, user-friendly IIoT solution – a solution which provides so much more than just the logging of data signals.