
Shifting dark, unstructured content to the cloud, data lakes, new systems and repositories will not give you the insights to compete in the new era. Let Adlib give you a head-start with intelligent data.
Adlib’s solution leverages automation and AI to discover, clean, classify and tag your unstructured content — including contracts with rich metadata — to make it easier to find, improve and leverage for downstream workflows.
Adlib gives you complete access and control over your document content and metadata, offering new data-driven insights and AI-powered categorization.
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.
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