Medical Devices
Instead of weeks of dedicated time I spent 20 hours of review time. For me the validation process was a really positive experience. It was seamless.
Cheryl Wagoner, Quality Manger, TranS1
Medical device manufacturing requires a meticulous adherence to details: the details of FDA regulations, 21CFR Part11, and FDA validation, among others. Selecting the ERP system and provider you can trust to manage your business requires the same attention.
You need a system with required functionality, such as traceability, provided by people who understand the challenges of manufacturing in an FDA regulated environment:
The commitment we saw from SoftBrands to make the implementation work, but also acknowledging the importance of validation, compared to what we saw with the competition was night and day.
Greg Manson, IT Director, TranS1
FourthShift Edition and SAP Business One.
Though some may offer the functionality you need, none have the ability to validate your implementation and processes as quickly and with as little investment required as SoftBrands.
FDA Validation made painless
The FDA validation procedure is painstaking and tedious. It drains a company of people, resources and money, and is often left incomplete.
SoftBrands offers you a noninvasive cure.
The SoftBrands validation team executes the protocols freeing your team to focus on normal routines. Because of this unique service, most are able to achieve validation in just a few weeks without disrupting their software implementation and with minimal staff time required.
View a demo of FourthShift Edition for Medical Device Manufacturers.
