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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
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