
Expedite customer-facing processes and create a data-driven mailroom analytics strategy. Bring automation to critical workflows, improve efficiencies and delight customers — that’s the Adlib digital mailroom.
Mobilize and structure data hidden in email and attachments to feed your workflows and repositories. Using intelligent data, you can automatically onboard new customers and suppliers, approve customer claims, and feed analytics engines.
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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1-866-991-1705
215-3228 South Service Road
Burlington, Ontario
L7N 3H8
Canada