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AI platform for regulatory submissions, INDs and health authority questions
Updated
Weave Bio is an AI platform for drug development teams that keeps source data, documents and regulatory context connected across submissions. It serves biotech, pharma and CRO teams.
Teams connect source documents and data, and Weave drafts submission content while keeping each statement traceable to its source. Reviewers collaborate in the platform, and the HAQ Manager helps respond to questions from health authorities.
Regulatory affairs and clinical teams at biotech, pharma and CROs use Weave to prepare submissions faster. The vendor reports 12 FDA submissions completed, 60% overall timeline compression and 50+ programs supported.
Weave Bio does not list prices. A free trial is listed; contact the vendor for plans.
H1 is a platform for healthcare professional data and engagement. PathAI applies AI to pathology. Latent Health helps clinical teams with documentation, so none of the listed alternatives matches Weave's regulatory submission focus.
Pricing Model
Subscription
Starting Price
Contact vendor
Free Options
Free trial
Weave Bio for individuals and growing teams. See weave.bio for current pricing.
Weave Bio for larger organizations with security and admin needs. Contact sales for a quote.
| Feature | Pro Popular | Enterprise |
|---|---|---|
| IND and submission drafting | , | |
| Document review | , | |
| Higher usage limits | , | |
| Integrations | , | |
| Email support | , | |
| Everything in Pro | , | |
| Source traceability | , | |
| Collaboration | , | |
| SSO and admin controls | , | |
| Dedicated support | , |
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API Types
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Developer Features
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Compliance Standards
SOC 2 Type II
EnterpriseISO 27001
EnterpriseGDPR Compliant
GlobalHIPAA
HealthcarePCI DSS
FinanceCCPA
PrivacyFedRAMP
GovernmentCSA STAR
CloudDeployment & Data
Data Residency Options
Verify with vendor for your specific region requirements.
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