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ease
features
design
support

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Description

The Multum database, which encompasses drugs, herbal remedies, and nutraceuticals, stands as a premier resource in the industry aimed at promoting safe medication practices and preventing harmful drug interactions. Its software solutions and databases deliver essential drug information, empowering clinicians to recommend appropriate medications with precise dosages while addressing potential interactions effectively. Lexicon Plus serves as a foundational database, offering extensive drug product and disease terminology that seamlessly connects to our clinical systems and external databases. Additionally, the VantageRx Database is designed in a Microsoft Access format, allowing integration into your applications and providing vital clinical information through multiple database tables. Organizations benefit from development interfaces, ensuring that their unique requirements are addressed. By allowing third-party applications to incorporate specialized functionalities into our software through an open and secure platform, we strive to enhance usability and meet diverse client needs. This integration ultimately aims to improve patient safety and healthcare outcomes.

Description

adWATCH - AE is a solution designed to aid pharmaceutical companies in handling and documenting adverse events that arise during clinical trials. It provides a quick and efficient way for reporters at clinics, hospitals, or investigative sites to create and oversee Adverse Event Reports (AERs), ensuring proper reporting to regulatory bodies and government organizations. An adverse effect refers to a harmful or undesirable reaction experienced by a patient due to medications or medical devices. The process of documenting adverse events necessitates thorough tracking of all medical complaint case details, which culminates in the creation of MedWatch reports, CIOMS reports, and other management documentation. With adWATCH - AE, researchers, physician investigators, Contract Research Organizations (CROs), clinical trial experts, and various health professionals can easily generate and submit AERs in compliance with FDA requirements, adhering to both MedWatch and CIOMS formats. This streamlined process not only enhances regulatory compliance but also improves patient safety oversight during clinical trials.

API Access

Has API

API Access

Has API

Screenshots View All

Screenshots View All

Integrations

Microsoft Access
Oracle Health

Integrations

Microsoft Access
Oracle Health

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

Oracle

Country

United States

Website

www.oracle.com/health/clinical-suite/electronic-health-record/#rc30p4

Vendor Details

Company Name

Atlant Systems

Website

atlantsystems.com/atlant/solutions/atwatch-ae/

Product Features

Product Features

CAPA

Audit Management
CAPA Planning
Change Management
Complaint Management
Incident Management
Nonconformance Tracking
Quality Control
Risk Management
Root Cause Analysis
Training Management

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