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

Pricing

Free Trial:
Free Trial available.

Integrations

API:
Yes, ClinVigilant offers API access

Ratings/Reviews

Overall 0.0 / 5
ease 0.0 / 5
features 0.0 / 5
design 0.0 / 5
support 0.0 / 5

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Company Information

ClinVigilant
Founded: 2017
United Kingdom
www.clinvigilant.com

Videos and Screen Captures

eTMF

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

Q: What kinds of users and organization types does ClinVigilant work with?
Q: What languages does ClinVigilant support in their product?
Q: What kind of support options does ClinVigilant offer?
Q: What other applications or services does ClinVigilant integrate with?
Q: Does ClinVigilant have an API?
Q: Does ClinVigilant have a mobile app?
Q: What type of training does ClinVigilant provide?
Q: Does ClinVigilant offer a free trial?

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

ClinVigilant Additional Categories