Global Pharmaceutical Promotional Content PlatformMulti-Market Compliance | 75% Faster Reviews
AI-powered platform for creating compliant pharmaceutical promotional materials across FDA, EMA, MHRA, Health Canada, and TGA markets. Automated claim extraction, PubMed reference linking, and built-in regulatory compliance checking for medical affairs and regulatory teams worldwide.
One Platform, Multi-Market Compliance
Create promotional materials that meet regulatory requirements across FDA, EMA, MHRA, Health Canada, and TGA markets. Built for global pharmaceutical companies and medical affairs teams.
Accelerate MLR Workflows by 75%
AI-powered claim extraction and automated reference linking reduce medical legal regulatory review cycles from 3 weeks to 3-5 days. Focus on medical strategy, not manual document review.
FDA Compliance Automation
Automated compliance checking against FDA promotional material guidelines, OPDP regulations, and PhRMA code standards. Built-in audit trails for regulatory submissions.
Cross-Functional MLR Collaboration
Streamline collaboration between medical affairs, legal, regulatory, and medical writing teams. Real-time review workflows with complete audit trails for documentation.
Trusted by Medical Affairs Professionals
Join teams creating compliant promotional content faster
“This platform has completely changed our workflow. The automated claim extraction and reference linking saves us countless hours, and the compliance checking gives us confidence that our materials meet all regulatory requirements.”
“The collaboration features and audit trail capabilities make cross-functional review seamless. Our legal, regulatory, and medical teams can all work together efficiently while maintaining full documentation.”
Ready to Transform Your Promotional Content Process?
Join hundreds of medical affairs professionals who have streamlined their workflow with PromoPack. Start your free trial today.
Frequently Asked Questions
Everything you need to know about PromoPack
What is PromoPack?
PromoPack is an AI-powered platform designed for pharmaceutical companies to create, review, and manage promotional content with built-in FDA compliance, automated claim extraction, and intelligent reference linking.
Is PromoPack FDA compliant?
Yes, PromoPack is built with FDA regulations in mind. Every document is automatically checked against FDA guidelines and industry standards. The platform includes compliance checking, audit trails, and regulatory review workflows.
How long does it take to review promotional materials?
PromoPack reduces review cycles by up to 75%. What traditionally takes 3 weeks can be completed in 3-5 days with automated claim extraction, reference linking, and collaborative review tools.
Can I try PromoPack before purchasing?
Yes! PromoPack offers a free demo mode where you can explore the platform with sample projects. No credit card or account required to try the demo.
What type of pharmaceutical companies use PromoPack?
PromoPack is used by medical affairs teams, regulatory affairs departments, and medical writers at pharmaceutical and biotechnology companies of all sizes, from startups to large enterprises.
Is my data secure with PromoPack?
Yes, PromoPack is HIPAA compliant and uses enterprise-grade security. All data is encrypted in transit and at rest, with comprehensive access controls and audit logging.
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