
Intelligent Document Processing surfaces data from unstructured documents, empowering businesses to operate more efficiently, identify risk, and improve customer experiences to gain a competitive edge.
FDA and other global regulators demand high-quality electronic submissions to approve new drugs and devices from Life Sciences leaders. Creating perfect PDF submission content manually was slow, inconsistent and expensive – delaying approvals and reducing time in market under patent.
Adlib delivers industry leading and fully automated PDF transformation and enhancement capabilities reducing costs, improving quality and ensuring consistency for submissions content enabling regulators to easily navigate and approve submissions.
FDA and other global regulators demand high-quality electronic submissions to approve new drugs and devices from Life Sciences leaders. Creating perfect PDF submission content manually was slow, inconsistent and expensive – delaying approvals and reducing time in market under patent.
Adlib delivers industry leading and fully automated PDF transformation and enhancement capabilities reducing costs, improving quality and ensuring consistency for submissions content enabling regulators to easily navigate and approve submissions.
FDA and other global regulators demand high-quality electronic submissions to approve new drugs and devices from Life Sciences leaders. Creating perfect PDF submission content manually was slow, inconsistent and expensive – delaying approvals and reducing time in market under patent.
Adlib delivers industry leading and fully automated PDF transformation and enhancement capabilities reducing costs, improving quality and ensuring consistency for submissions content enabling regulators to easily navigate and approve submissions.
FDA and other global regulators demand high-quality electronic submissions to approve new drugs and devices from Life Sciences leaders. Creating perfect PDF submission content manually was slow, inconsistent and expensive – delaying approvals and reducing time in market under patent.
Adlib delivers industry leading and fully automated PDF transformation and enhancement capabilities reducing costs, improving quality and ensuring consistency for submissions content enabling regulators to easily navigate and approve submissions.
Today's innovators use proven technology to surface critical data from multiple sources and unstructured document formats to drive analytics, content services (ECM), robotic process automation (RPA), insight platforms, and business process management (BPM) systems.
Life sciences and pharma leaders must continually evaluate their operations and technology, surface siloed data, fix broken and legacy systems, and address growing compliance concerns. Adlib’s Document Transformation platform powers Intelligent Document Processing and fuels digital transformation, helping pharma and life sciences leaders accelerate FDA submissions, improve data privacy, and overcome R&D roadblocks.
Large banks spend up to 500 million a year to ensure customers are who they claim to be, and KYC-related fines against banks totaled $26 billion over the past 10 years. To protect customers’ personally identifiable information (PII) and deliver a delightful, digital experience, banks must replace broken and legacy processes with simple, sophisticated digital workflows. Adlib’s Document Transformation platform fuels Intelligent Document Processing to turn this vision into reality.
To outcompete digital upstarts, insurers must deliver fast, empathetic, light-touch support as a point of differentiation. Yet only a fraction of insurers have fully automated claims processing. Adlib transforms documents in 300+ formats into easy-to-consume data that feeds into downstream systems, technologies, and workflows. By fueling Intelligent Document Processing to accelerate claims and other data-heavy processes, Adlib allows your team to focus on what they do best: being human.
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