Shortlist drug-manufacturing partners, run RFIs, and close in a secure dealroom — on a directory screened against live FDA recalls, Warning Letters, and Form 483 observations, refreshed weekly.
7 days free · Card required · Cancel anytime before it ends
Aggregated & verified from official registries
Hours spent scrubbing ClinicalTrials.gov, FDA databases, and press releases.
Judging CDMO capabilities based on outdated PDFs and marketing claims.
Losing out on licensing deals because the signal was buried in noise.
Spreadsheets, emails, and PDFs...
Stop jumping between FDA databases, supplier PDFs, and email threads. PharmaTek brings discovery, compliance screening, and RFIs into a single sourcing workspace.
Find CMOs, CDMOs, and API suppliers with the right capabilities — then shortlist and RFI them in seconds.
Screen partners against FDA recalls, Warning Letters, and Form 483s — and get alerted when new enforcement signals land.
Market Snapshot
From raw data to actionable deal flow in five steps.
Ingest structured data from trusted public registries (FDA, ClinicalTrials.gov, PubMed) and PharmaTek enrichment pipelines.
Our AI engine cleans, structures, and links data to create a unified entity graph.
Automated checks against trusted sources ensure you make decisions on accurate data.
Search, filter, and discover partners or assets using our advanced intelligence tools.
Shortlist candidates, launch RFIs, and manage deals directly within the platform.
A comprehensive suite of intelligence tools designed for every stage of the pharma lifecycle.
Sourcing Workspace
Run sourcing end to end: shortlist CMOs, CDMOs, and API suppliers, send secure RFIs, and compare responses side by side — all in one project workspace.
Learn more →
Company & CDMO Finder
Search 22,000+ pharma companies, biotechs, CDMOs, CMOs, and API suppliers. Filter by geography and type, with verification badges and FDA compliance flags before you engage.
Learn more →
FDA Compliance Screening
Vet partners against 4,000+ FDA enforcement signals — drug recalls, Warning Letters, and Form 483 observations — with recency-aware risk bands so you spot elevated risk before you contract.
Partner Network
Map relationships between sponsors, CROs, and CDMOs across 600+ verified partners. Surface the supply-chain ecosystem behind every asset.
Learn more →
Secure Dealroom
Invite shortlisted suppliers into a secure, token-gated response portal — they submit RFI/RFQ answers and quotes without an account, and you compare every response side by side.
Learn more →
API & Molecule Sourcing
Search 2,500+ active pharmaceutical ingredients to find and qualify suppliers. Regulatory and supplier fields continue to expand; coverage varies by compound.
Learn more →
Facilities Directory
Browse 1,000+ manufacturing sites with capability and certification fields where enriched. Full per-facility inspection history is on the roadmap.
Learn more →
Clinical Trials Explorer
Explore 12,000+ clinical trials from public registries (ClinicalTrials.gov and ISRCTN), refreshed weekly. Analyze sponsors, phases, and investigators with verification badges where available.
Learn more →
Global Drug Pipeline
Track development status across thousands of assets and all clinical phases. Filter by therapeutic modality, route of administration, and verification status.
Learn more →
Competitive Intelligence
Monitor competitor pipelines, strategic deals, and clinical milestones. Track risks and emerging opportunities with AI-assisted summaries.
Learn more →
Dossier Marketplace (Preview)
60,000+ regulatory filings across the FDA (Drugs@FDA) and UK MHRA (NHS dm+d) — product, active substance, MA holder and status. Useful for discovery; the licensing marketplace is still preview.
Learn more →
PharmaTek AI Assistant
Chat with your data. Ask complex questions about partners, market trends, competitor analysis, and document summaries.
Learn more →
Sequences & Activity
Automated outreach with Resend integration. Track open rates and engagement across your sourcing and BD campaigns.
Learn more →
We don’t just scrape web pages. We integrate directly with structured government and scientific registries, cross-checking every record against its source to catch stale or conflicting data before you see it.
The only platform that combines public data aggregation with AI-driven normalization and verification.
Vet partners against 4,000+ FDA enforcement signals — recalls, Warning Letters, and Form 483 observations — with recency-aware risk bands across the directory and your sourcing projects.
Automated ingestion jobs refresh clinical trials, companies, partners, and FDA signals weekly — your data is a live feed, not a static snapshot.
We link entities (companies, drugs, trials, patents) into a unified knowledge graph.
UK-GDPR compliant, with row-level tenant isolation and a Data Processing Agreement available for procurement review.
Whether you are hunting for assets or de-risking supply chains, PharmaTek adapts to your workflow.
De-risk your supply chain. Shortlist and qualify CMO/CDMO/API suppliers, screen FDA compliance, and run RFIs before you engage.
Selecting a biologics CDMO turns on platform and expression-system fit, real analytical characterization depth, and demonstrated regulatory experience with your modality — not headline bioreactor capacity. A practical framework for mAbs and recombinant proteins.
Cell and gene therapy manufacturing is defined by the sub-modality — viral vector, autologous or allogeneic cell therapy — and by two hard problems: potency analytics and logistics. How to select a CGT CDMO without buying the wrong kind of capability.
Find, vet, and source drug-manufacturing partners faster — with FDA compliance screening built in. Start free for 7 days.