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Average Ratings 0 Ratings

Total
ease
features
design
support

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Write a Review

Description

AnjuEPS stands out as a premier solution for eSource and site automation, specifically crafted to enhance the efficiency of early-phase clinical trials, encompassing everything from the recruitment of volunteers to the final submission of studies. By capturing data directly from medical devices and implementing real-time edit checks, it guarantees the accuracy of data while eliminating reliance on traditional paper sources. The platform enhances safety monitoring with real-time alerts for out-of-range values and provides insights through historical safety data, ultimately facilitating improved management of volunteer safety. Its user-friendly Design & Build Module significantly accelerates the study setup process, which in turn helps lower both time and financial expenditures. Among its notable features are ad hoc reporting capabilities, sample tracking for intricate pharmacokinetic and pharmacodynamic activities, and comprehensive modules for recruitment and pharmacy management. With AnjuEPS, the collection of clinical data is not only efficient but also characterized by high levels of accuracy and transparency, making it an invaluable resource for clinical researchers. The solution's ongoing updates ensure that it remains at the forefront of technological advancements in the clinical trial landscape.

Description

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. Every interaction and data exchange creates Audit Trails, which provide compliant real-time data visibility across all relevant roles. Our products are modular, highly customizable, and available on the web, iPad, and Mobile App for both Android and iOS. We also support Patient's Own Device (BYOD) and interface with Devices and Wearables. Clinvigilant💊, your one-stop🌐solutions provider for clinical trials☁️ .

API Access

Has API

API Access

Has API

Screenshots View All

Screenshots View All

Integrations

Medidata
Medrio
OpenClinica
Oracle API Catalog
REDCap
Veeva Vault
Zelta

Integrations

Medidata
Medrio
OpenClinica
Oracle API Catalog
REDCap
Veeva Vault
Zelta

Pricing Details

No price information available.
Free Trial
Free Version

Pricing Details

No price information available.
Free Trial
Free Version

Deployment

Web-Based
On-Premises
iPhone App
iPad App
Android App
Windows
Mac
Linux
Chromebook

Deployment

Web-Based
On-Premises
iPhone App
iPad App
Android App
Windows
Mac
Linux
Chromebook

Customer Support

Business Hours
Live Rep (24/7)
Online Support

Customer Support

Business Hours
Live Rep (24/7)
Online Support

Types of Training

Training Docs
Webinars
Live Training (Online)
In Person

Types of Training

Training Docs
Webinars
Live Training (Online)
In Person

Vendor Details

Company Name

Anju Software

Founded

2016

Country

United States

Website

www.anjusoftware.com/eclinical/anjueps/

Vendor Details

Company Name

ClinVigilant

Founded

2017

Country

United Kingdom

Website

www.clinvigilant.com

Product Features

Electronic Data Capture

Audit Trail
CRF Tracking
Data Entry
Data Verification
Distributed Capture
Document Imaging
Document Indexing
Forms Management
Remote Capture
Study Management

Product Features

Clinical Trial Management

21 CFR Part 11 Compliance
Document Management
Electronic Data Capture
Enrollment Management
HIPAA Compliant
Monitoring
Patient Database
Recruiting Management
Scheduling
Study Planning

Electronic Data Capture

Audit Trail
CRF Tracking
Data Entry
Data Verification
Distributed Capture
Document Imaging
Document Indexing
Forms Management
Remote Capture
Study Management

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