Pharma Marketing Operations Digital Worker

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What this Digital Worker does:

The Pharma Marketing Operations Digital Worker accelerates compliant promotional content review across global medical, legal, and regulatory teams. It pre-screens draft assets, identifies claim risks, and proposes compliant rewrites before human review.

By transforming fragmented MLR workflows into a transparent, auditable process, it enables faster campaign releases, higher reviewer throughput, and stronger governance across all promotional channels and markets.

journey

Faster Campaign Approvals: Automated pre-checks remove obvious compliance issues, flagging only novel changes for review—compressing approval cycles from weeks to days.

message

Higher Reviewer Throughput: Automated claim detection, citation matching, and comment consolidation free experts from repetitive checks, enabling more assets per reviewer.

layers

Improved Compliance Quality: Consistent rules and traceable line-level citations reduce late-stage defects, audit findings, and regulatory follow-up across global submissions.

The Problems This Digital Worker Solves

Slow MLR Cycles

Manual, multi-week review loops delay launches and reduce revenue potential as teams chase incremental approvals across functions.

Repetitive, Low-Value Tasks

Skilled reviewers spend excessive time re-reading, comparing versions, and checking label alignment instead of focusing on judgment-based work.

Audit and Traceability Gaps

Dispersed comments, unclear rationale, and missing version histories create compliance risks during audits and regulatory inspections.

The Technical Make-Up

This Digital Worker is a multi-agentic system, with pioneering technology built in, and tailored specifically to your organization's guardrails, outcomes, and objectives.

The Multi-Agent Workflow:

Collects draft materials from content systems, freezes versions, and links them to the latest approved labels and policies.

Integrations:

  • Veeva Vault PromoMats

  • Adobe Experience Manager and other DAM platforms

  • PubMed and internal reference libraries

  • Label management and approved claims repositories

  • Identity and workflow management systems

What It Replaces & Reduces:

  • Manual pre-screening and redundant review cycles

  • Email-based routing and fragmented comment tracking

  • Re-reads of unchanged materials between submissions

  • Unstructured audit preparation and evidence collation

  • Late-stage compliance corrections and rework