Enterprise-Grade Pricing forPharmaceutical Innovation
Plans designed to scale with your organization—from individual contributors to global enterprises.
Every plan includes claim extraction, evidence linking, pack export, and a language risk scan. Human MLR review always required.
Starter
For individual medical writers and consultants
Professional
For medical affairs and agency teams
Business
For growing pharmaceutical companies
Enterprise
For large pharma with complex needs
Important: Please Read Before Purchasing
This is a workflow assistant tool, not a compliance guarantee system
⚠️ Human Review Always Required
All system-generated suggestions must be reviewed by qualified medical affairs, legal, and regulatory professionals. This tool assists with data entry but does not replace human judgment.
⚠️ No Compliance Guarantee
This software does not guarantee regulatory compliance. Your organization is responsible for ensuring all promotional materials meet FDA, EMA, MHRA, and other applicable regulatory requirements.
⚠️ Early Access Product
This is an actively-developed product. Features may change, and we recommend pilot testing with non-critical projects first. We are seeking feedback from early users.
⚠️ Legal Review Required
Your legal, regulatory, and IT teams should review and approve this tool before use. We recommend running a security assessment and establishing clear SOPs for tool usage.
Calculate Your ROI
At £75/hour (average pharma labor cost), that's £1,125 saved per pack.
The Professional plan pays for itself with just 1 pack per month. The Enterprise plan delivers £100K+ annual savings for large teams.
Premium Database Integrations
Expand your research capabilities with access to leading medical databases. Available as add-ons to Professional, Business, and Enterprise plans.
EMBASE
Access 32M+ biomedical records. Comprehensive pharmaceutical and biomedical literature coverage with 90% overlap reduction vs PubMed.
- 32M+ biomedical records
- Drug & device indexing
- European focus
Cochrane Library
Gold standard for systematic reviews and meta-analyses. High-quality evidence synthesis for regulatory submissions.
- 10K+ systematic reviews
- Clinical trial registry
- Evidence-based medicine
Regional Bundle
Access regional databases for Asia-Pacific, Latin America, and emerging markets. Essential for global expansion.
- J-STAGE (Japan)
- SciELO (Latin America)
- CNKI (China)
All database integrations include API access, automated reference matching, and full-text linking where available.
Sound Familiar?
Spending days assembling claims and PDFs into a reference pack
Guided extract → review → link → export workflow
Hunting through PubMed for supporting references
PubMed search suggests candidates you can accept or reject
Missing a claim–reference link before MLR
Link status is visible before you generate the pack
Recreating the same reference pack structure every time
Reusable project templates to get started faster
Help Us Build a Better MLR Workflow Tool
We're actively developing this platform and looking for pharmaceutical professionals to provide feedback. Early adopters get priority support and significant influence on feature development.
No credit card required for demo • Full refund within 30 days if not satisfied
Still Have Questions?
Can I cancel anytime?▼
Yes! Cancel with one click. No contracts, no hassle. Full refund within 30 days.
What if I need more packs?▼
Upgrade instantly or purchase additional packs as needed with overage billing.
Is my data secure?▼
We use enterprise-grade encryption and secure cloud storage. However, you should conduct your own security assessment before uploading sensitive data.
Does this guarantee regulatory compliance?▼
No. This is a workflow tool that assists with documentation. Your medical affairs, legal, and regulatory teams are responsible for ensuring compliance. Human review is always required.
Who should review this tool before we use it?▼
We recommend review by your legal, regulatory affairs, IT security, and medical affairs departments. We can provide documentation to support their review process.
What if the system makes a mistake?▼
All suggestions must be reviewed by humans. We provide this tool 'as-is' and users are responsible for validating all output. See our Terms of Service for details.
Ready to Get Your Time Back?
Join teams who've already automated their promotional material workflow.
✓ 14-day free trial ✓ No credit card required ✓ Cancel anytime