The |
for Pharma & Biotech

Unify pipeline intelligence, competitive analysis, market data, and business development in one enterprise-grade AI platform.

Intelligence aggregated from global sources

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The Old Way of
Pharma Sourcing

Fragmented Data

Hours spent scrubbing ClinicalTrials.gov, FDA databases, and press releases.

Manual Verification

Judging CDMO capabilities based on outdated PDFs and marketing claims.

Missed Assets

Losing out on licensing deals because the signal was buried in noise.

🤯

Spreadsheets, emails, and PDFs...

Unified Intelligence

One Platform.
Infinite Insights.

Stop jumping between FDA databases, clinical registries, and news feeds. PharmaTek brings every data point into a single, searchable command center.

Real-Time Surveillance

Get alerts the moment a competitor updates a trial or files a new patent.

Partner Discovery

Find CDMOs with available capacity and specific technical capabilities in seconds.

Search for companies, drugs, or trials...

Market Snapshot

Oncology (Solid Tumor)

GlobalPhase II+
Active Trials
Approvals
Deals
Curis Inc.
Phase III
+12%
Replimune
Phase II
+4%
Iovance
BLA Filed
+28%

How It Works

From raw data to actionable deal flow in five steps.

01

Ingest & Integrate

Connect your existing subscriptions (IQVIA, Clarivate) alongside our proprietary global signals.

02

Normalize

Our AI engine cleans, structures, and links data to create a unified entity graph.

03

Verify

Automated checks against trusted sources ensure you make decisions on accurate data.

04

Explore

Search, filter, and discover partners or assets using our advanced intelligence tools.

05

Execute

Shortlist candidates, launch RFIs, and manage deals directly within the platform.

Core Modules

A comprehensive suite of intelligence tools designed for every stage of the pharma lifecycle.

PharmaTek AI Assistant

Chat with your data. Ask complex questions about market trends, competitor analysis, and document summaries.

Natural Language Queries
Document Analysis
Market Citations

Competitive Intelligence

AI-powered monitoring of competitor pipelines, deals, and strategic moves. Track risks and opportunities in real-time.

Strategic Focus Analysis
Key Development Alerts
Risk/Opportunity Scoring

Global Drug Pipeline

Track development status across all phases. Filter by modality, route of administration, and verification status.

Modality Filtering
Commercial Revenue Data
Pipeline Stage Tracking

Company & CDMO Finder

Global database of 10,000+ pharma companies, biotechs, CDMOs, and CMOs. Filter by capabilities, certifications, and location.

Capability Verification
Regulatory History
Capacity Indicators

Facilities Directory

Deep dive into manufacturing sites. Verify GMP status, inspect FDA warning letters, and assess production scale.

FDA/EMA Inspection Logs
Production Line Analysis
Site-Level Certifications

API & Molecule Sourcing

Sourcing intelligence for small molecules and biologics. Track suppliers, USDMF availability, and regulatory context.

USDMF Status
Supplier Tiers
Patent Expiry Tracking

Dossier Marketplace

Marketplace intelligence for ready-to-license dossiers (NDA/BLA/ANDA). Identify ownership signals and availability.

CTD Availability
Zone IVb Stability
Bioequivalence Studies

Clinical Trials Explorer

Real-time surveillance of 50,000+ clinical trials. Analyze sponsors, investigators, and recruitment status.

Investigator Performance
Site Selection Intelligence
Competitor Benchmarking

Partner Network

Map relationships between sponsors, CROs, and CDMOs. Visualize the unseen supply chain ecosystem.

Supply Chain Mapping
Partnership History
Vendor Risk Scoring

Sourcing Workspace

End-to-end RFI/RFP management. Shortlist vendors, send secure inquiries, and track responses in one place.

Multi-Vendor RFIs
Response Comparison
Project Timelines

Secure Dealroom

Tokenized, audit-logged data rooms for secure asset sharing and due diligence during licensing deals.

Access Tracing
Watermarking
Expiry Controls

Sequences & Activity

Automated outreach with Resend integration. Track open rates and engagement for your BD campaigns.

Automated Follow-ups
Engagement Scoring
CRM Sync

Built on the World’s Most Trusted Data

We don’t just scrape web pages. We integrate directly with structured government and scientific registries, validating data across multiple touchpoints to remove hallucinations and outdated records.

ClinicalTrials.gov
Registry
FDA Orange Book
Regulatory
EMA EudraCT
Registry
Corporate Filings (SEC)
Financial
PubMed / Medline
Scientific
Patent Offices (USPTO/WIPO)
IP
Raw Sources
Unstructured & Fragmented
10M+ Records
AI Normalization Layer
Verified Intelligence
Structured & Actionable
Ready for Query

Why PharmaTek?

The only platform that combines public data aggregation with AI-driven normalization and verification.

Verified Intelligence

We don't just aggregate; we verify. Every data point is checked against regulatory filings.

Real-Time Updates

Clinical trials and regulatory changes are synced hourly, not quarterly.

Deep Graph Data

We link entities (companies, drugs, trials, patents) into a unified knowledge graph.

Enterprise Security

SOC 2 compliant infrastructure with row-level security and strict data isolation.

Built for Every Stakeholder

Whether you are hunting for assets or de-risking supply chains, PharmaTek adapts to your workflow.

BD Manager

Accelerate deal flow by identifying licensing opportunities and capable partners 10x faster.

Find in-licensing assets
Qualify leads instantly
Track competitor activity

Frequently Asked Questions

Ready to Accelerate Your
Discovery Workflow?

Join thousands of BD professionals and researchers using PharmaTek to find, verify, and source assets faster.