Audience
CRO, Pharma, Biotech, Academia, Medical Devices and Research institutions conducting clinical trials.
About ClinVigilant
Streamline your clinical studies with Clinvigilant, your global cost-effective eClinical tools provider for CROs, Pharma, Biotech, Nutraceuticals and Academic organizations in clinical and post-marketing stages. Most of our clients choose and stay with us for thanks to our:
♦ Fast EDC set-up (less than 4 weeks).
♦ Cost-effectiveness.
♦ 3rd party integrations (including legacy systems).
Our cloud-based suite (Microsoft Azure) is HIPAA, ICH-GCP, GDPR & 21 CFR part 11 compliant and we have been audited by the FDA, EMA and MHRA.
The Clinvigilant eClinical suite includes: EDC, CTMS, eCRF, eTMF, eSource, IWRS, ePRO, eConsent and eCOA. Just pick the tools that you need and we will integrate them within your existing software ecosystem.
How simple and user-friendly is it? Ask for a demo to find out!
Clinvigilant💊, your one-stop 🌐solutions provider for ☁️clinical trials.
Enquiries > bd (at) clinvigilant.com
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Pricing
Free Trial:
Free Trial available.
Company Information
ClinVigilant
Founded: 2017
United Kingdom
www.clinvigilant.com
Videos and Screen Captures
eTMF
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Product Details
Platforms Supported
Cloud
Windows
iPhone
iPad
Android
On-Premises
Training
Documentation
Live Online
Webinars
Support
Phone Support
24/7 Live Support
Online
ClinVigilant Frequently Asked Questions
ClinVigilant Product Features
Clinical Trial Management
21 CFR Part 11 Compliance
Document Management
Electronic Data Capture
Enrollment Management
HIPAA Compliant
Monitoring
Scheduling
Study Planning
Patient Database
Recruiting Management
Electronic Data Capture
Audit Trail
CRF Tracking
Data Entry
Data Verification
Forms Management
Remote Capture
Study Management
Distributed Capture
Document Imaging
Document Indexing
