Medical Affairs Solutions

Medical Affairs Software That Actually Understands Your Workflow

Purpose-built for medical affairs teams managing pharmaceutical promotional content. Automate MLR reviews, streamline cross-functional collaboration, and maintain FDA compliance—all in one platform.

The Medical Affairs Challenge

Slow MLR Review Cycles

3-4 week review cycles delay product launches and marketing campaigns. Manual claim extraction and reference verification bottleneck your team.

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Compliance Risk

Manual compliance checking leads to errors. FDA OPDP citations cost companies millions in corrective actions and reputation damage.

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Siloed Workflows

Medical, legal, and regulatory teams work in separate systems. Version control nightmares and lost audit trails create chaos.

How PromoPack Transforms Medical Affairs

Purpose-built for the unique needs of pharmaceutical medical affairs teams

Automated MLR Workflow

AI-powered claim extraction automatically identifies all product claims in your promotional materials. Smart reference linking matches claims to supporting literature. Compliance pre-checks flag potential FDA issues before legal review.

  • Reduce review cycles from 3 weeks to 3-5 days
  • Automated claim-reference validation
  • Real-time compliance checking
75%
Faster Review Cycles
99%
Compliance Accuracy

Built-In FDA Compliance

Every document is automatically validated against FDA OPDP regulations, PhRMA code, and your internal compliance policies. Complete audit trails ensure regulatory readiness.

  • OPDP regulation checking
  • Fair balance verification
  • Complete audit trail documentation

Cross-Functional Collaboration

Unified platform for medical affairs, legal, regulatory, and marketing teams. Real-time collaboration, role-based permissions, and intelligent workflow routing keep everyone aligned.

  • Real-time collaborative review
  • Automated workflow routing
  • Version control and approval tracking
50+
Hours Saved Per Month

Complete Medical Affairs Toolkit

Claim Extraction

AI automatically identifies all product claims

Reference Linking

Smart matching to PubMed and internal databases

Compliance Checking

Real-time FDA OPDP regulation validation

MLR Workflow

Automated routing to medical, legal, regulatory

Audit Trails

Complete documentation for regulatory submissions

Team Collaboration

Real-time review and approval workflows

Ready to Transform Your Medical Affairs Workflow?

See how PromoPack can reduce your MLR review cycles by 75%

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