PharmaCopilot
by PharmaCopilot Inc
Accelerate drug discovery documentation with AI-powered research assistance
Cambridge, MA10-49 employeesFounded 2021Updated 11/20/2024
4.3
Based on 41 reviews
About
PharmaCopilot assists pharmaceutical researchers with literature review, clinical trial documentation, and regulatory submission preparation. It ensures compliance with FDA 21 CFR Part 11 and streamlines the drug development lifecycle.
Key Features
Literature review automation
Clinical trial protocol writing
Regulatory submission prep
Adverse event monitoring
Data room management
Audit trail compliance
Integrations
Veeva VaultIQVIAMedidataTrialScope
User Reviews
Write a ReviewNo reviews yet. Be the first to review this tool!
Write a ReviewCompliance & Certifications
SOC 2
HIPAA
FDA 21 CFR Part 11
Industries
Use Cases
Deployment Options
CloudPrivate Cloud
Pricing
Enterprise
Support Options
- Phone
- Scientific advisors
Related Tools
Clinical Notes Pro
VerifiedMedScribe AI
4.7
127 reviews
AI-powered clinical documentation that saves physicians 2+ hours daily
SOC 2 Type IIHIPAAHITRUST
San Francisco, CA50-249 employees
Claims Intelligence
VerifiedInsureTech AI
4.5
95 reviews
Intelligent claims triage and fraud detection reducing processing time by 65%
SOC 2 Type IIISO 27001HIPAA
Chicago, IL250-999 employees
SecureChat Enterprise
VerifiedSecureComms
4.4
156 reviews
HIPAA-compliant messaging and collaboration for healthcare teams
SOC 2 Type IIHIPAAHITRUST
Nashville, TN50-249 employees