Revolutionizing PharmaceuticalContent Creation

We're on a mission to eliminate the bottlenecks in promotional material development, ensuring medical affairs teams can focus on science while maintaining perfect compliance.

Our Mission

In the pharmaceutical industry, time-to-market can mean the difference between helping patients and missing opportunities. Yet, creating compliant promotional materials remains a painfully manual process.

We believe medical affairs professionals should spend their time advancing science, not wrestling with paperwork. That's why we built PromoPack – to help assemble UK PMCPA reference packs: extract suggested claims, review them, link evidence, and export.

It is a workflow tool for medical writers and agencies—not a compliance system. Human MLR review always remains required.

UK
PMCPA pack focus
Human
Review required
4
Steps: extract → review → link → export
Demo
Try without signup

Our Story

Born from frustration, built for excellence

1

The Problem

Building a PMCPA reference pack in Acrobat—collating every claim and cited paper— is slow, tedious, and easy to get wrong. That admin work diverts medical writers and medical affairs teams from higher-value review.

2

The Solution

PromoPack assists with claim extraction, human review gates, reference linking, and pack export—so teams spend less time on dossier assembly and more time on real MLR judgement.

3

The Impact

We're early access and focused on the UK reference-pack job. If you build packs today and want a cleaner workflow, try the demo and tell us what still hurts.

Leadership Team

Industry veterans committed to transforming pharmaceutical content creation

SJ

Sarah Johnson

CEO & Co-Founder

Former Director of Medical Affairs at Pfizer with 15+ years in pharmaceutical regulatory affairs and promotional content development.

MR

Michael Rodriguez

CTO & Co-Founder

Former VP of Regulatory Technology at Novartis. Expert in intelligent/ML applications for life sciences and healthcare compliance automation.

AL

Amanda Liu

Head of Regulatory Affairs

Former FDA regulatory reviewer turned industry consultant. Ensures PromoPack meets the highest standards of pharmaceutical compliance and data integrity.

Our Values

The principles that guide everything we do

Compliance First

Every feature is designed with regulatory requirements in mind.

Innovation

We leverage cutting-edge intelligent tools to solve real industry challenges.

Collaboration

We work closely with our users to build the perfect solution.

Patient Focus

Everything we do ultimately serves patients and healthcare providers.

Join the PromoPack Revolution

Be part of the future of pharmaceutical content creation. Experience the difference PromoPack makes.