Streamline Your MLR Workflow withAI-Assisted Documentation
A workflow tool for pharmaceutical promotional content creation. AI-assists with claim extraction and reference linking. Human review always required.
Strengthen Pipelines. Power Transformation.
Comprehensive AI platform designed for life sciences. From target identification to regulatory submission, accelerate every stage of pharmaceutical content creation.
Streamline Documentation Workflows
AI-assists with claim extraction and reference linking to reduce manual data entry. All AI suggestions require human review. Focus on strategy, not tedious copy-paste.
Maintain Audit Trails
Track all document changes and reviews with built-in audit trails. Supports compliance documentation for FDA, EMA, MHRA, and other regulatory bodies.
Collaborative Review Workflows
Coordinate cross-functional teams with shared workspace. Medical affairs, legal, and regulatory teams can review documents together with comments and approval tracking.
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Help shape the future of pharmaceutical content workflows
Important: This is a Workflow Tool, Not a Compliance System
- •Human review is always required. AI assists with data extraction but cannot replace regulatory review.
- •Not a compliance guarantee. This tool supports documentation workflows but does not ensure regulatory compliance.
- •Early access product. We're actively developing features and gathering feedback from beta users.
- •Your legal/regulatory teams must approve. All pharmaceutical content requires proper MLR review regardless of tools used.
What This Tool Does
- Reduces manual data entry for claims and references
- Organizes documents in a structured workflow
- Maintains audit trails for documentation
- Facilitates team collaboration on reviews
What This Tool Does NOT Do
- Replace human regulatory review
- Guarantee FDA/EMA/MHRA compliance
- Make regulatory decisions for you
- Substitute for legal/medical affairs expertise
Looking for Early Adopters
We're seeking pharmaceutical consultants and small biotech companies to help us refine this tool. Early access users get significant input on feature development.
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Frequently Asked Questions
Everything you need to know about PromoPack
What is PromoPack?
PromoPack is a workflow tool for pharmaceutical teams creating promotional content. It helps organize documents, extract claims with AI assistance, and link to supporting references. All AI suggestions require human review.
Does PromoPack ensure regulatory compliance?
No. PromoPack is a workflow tool that helps organize documentation, but does not validate regulatory compliance. Your medical, legal, and regulatory teams must review all materials. The platform provides audit trails and version control to support your compliance processes.
How does PromoPack help with documentation?
PromoPack reduces time spent on manual tasks like copying claims and organizing references. AI assists with extracting information from documents, but all suggestions require review. Teams can collaborate on projects with shared workspaces and approval workflows.
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?
PromoPack uses industry-standard security practices. All data is encrypted in transit (HTTPS) and at rest, with access controls and audit logging. We're an early-stage product actively working toward enterprise certifications.
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