Intelligent Document Processing for Innovation in Life Sciences Regulations
Evi Cohen, Vice President, Global Life Sciences & Healthcare, Appian
August 13, 2020
In the wake of the COVID-19 pandemic, many life sciences organizations are seeking efficiency and control over the regulatory process more than ever before. There is an increased urgency for speed, accuracy, and simplified processes in the Regulatory Information Management (RIM) space, and to prioritize projects that will quickly deliver the most patient value.
Intelligent Document Processing for Regulatory Information Management
Appian Intelligent Document Processing (IDP) can ease the burden and stress of regulatory management by reducing manual effort and the potential for human error. Using machine learning and artificial intelligence on Appian's low-code automation platform they take the information you need, and automatically file it where it's needed as soon as it's in the system. This means real-time updating for regulations as they evolve and ensuring compliance isn't what's holding your product development back.
With Appian organizations have the flexibility to implement a fit for purpose RIM solution that will rapidly provide visibility and awareness across product development life cycles. Also, with IDP, the risk of redundant data is reduced and even exception handling can be routed through machine learning.
Appian is the unified platform for change. We accelerate customers’ businesses by discovering, designing, and automating their most important processes. The Appian Low-Code Platform combines the key capabilities needed to get work done faster, Process Mining + Workflow + Automation, in a unified low-code platform. Appian is open, enterprise-grade, and trusted by industry leaders.