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Description
QAPI360 is a comprehensive, cloud-based software solution designed for Quality Assurance Performance Improvement (QAPI) that complies with HIPAA regulations, enabling healthcare providers to centralize, organize, and monitor all aspects of their quality programs. By moving away from outdated spreadsheets and disjointed methods, agencies can adopt a systematic, data-driven framework that includes well-structured QAPI plans, quality metrics, and tracking for incidents involving patients and staff. The software also features infection control monitoring, logs for medication errors and adverse drug reactions, hand hygiene initiatives, templates for performance improvement projects, patient satisfaction assessments, and tracking of contracted provider performance, all displayed through interactive dashboards that allow users to identify trends, implement corrective measures, and evaluate results effectively. Additionally, QAPI360 simplifies data entry, supports EMR integration or automated data imports, and provides built-in reporting tools, which facilitate compliance documentation and audits while enhancing the efficiency of data collection, charting, and root-cause analysis processes. Ultimately, this software serves as a vital resource for healthcare agencies striving to enhance their quality assurance initiatives and ensure optimal patient care.
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
No details available.
Integrations
No details available.
Pricing Details
$249.99 per month
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
QAPI360
Country
United States
Website
qapi360.com
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