Medical Device manufacturers are required by the FDA to track certain types of devices from manufacture through the distribution chain to patients. The FDA released 21 CFR Part 821, which governs the requirements around the tracking process. Our DocuNECT solution is used by both large and small Medical Companies, in the cloud and on-premise.
More and more solution providers are offering cloud-based solutions, but are they offering technology or a solution…and what’s the difference?
This article provides a link to the ApplicationXtender Healthcare webinar held on 09/27/2018. Agenda A Digital Future The Solution – OpenText ApplicationXtender How Do I Get There? Recorded Webinar