Clario Pharmacovigilance Solutions
Delivering the evidence and insights to unlock transformative therapies.
Overview
Clario, which has integrated Bioclinica's safety solutions, offers a range of pharmacovigilance services and technologies. Their focus is primarily on managing safety within clinical trials. They provide solutions for adverse event reporting, case processing, safety database management, and regulatory submissions. Clario combines scientific expertise with technology to help sponsors ensure patient safety and regulatory compliance throughout the clinical development process.
✨ Key Features
- Clinical trial safety management
- Adverse event case processing
- Global safety database
- Regulatory reporting and submissions
- Signal detection and risk management
- Medical review and assessment services
🎯 Key Differentiators
- Deep focus on clinical trial technology and evidence generation
- Integration with a broad portfolio of clinical trial solutions (eCOA, Imaging, etc.)
- Combination of technology with deep scientific and regulatory expertise
Unique Value: Provides an integrated approach to clinical trial safety, combining technology and scientific expertise to ensure compliance and generate high-quality safety data.
🎯 Use Cases (3)
✅ Best For
- Supporting global clinical trials for pharmaceutical and biotech companies by managing their safety data and reporting obligations.
💡 Check With Vendor
Verify these considerations match your specific requirements:
- Companies focused solely on post-marketing pharmacovigilance might find the solution too centered on clinical development.
🏆 Alternatives
Offers tighter integration with other clinical trial endpoints and data sources (like eCOA and medical imaging) compared to standalone PV systems.
💻 Platforms
🔌 Integrations
🛟 Support Options
- ✓ Email Support
- ✓ Phone Support
- ✓ Dedicated Support (Varies tier)
🔒 Compliance & Security
💰 Pricing
Free tier: NA
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