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What is MEDAS HIMS?

MEDAS HIMS provides an all-encompassing web-based ERP software solution specifically designed for hospitals, regardless of their size, that enhances the quality of patient care while optimizing operational efficiency, promoting real-time data sharing, and improving revenue generation. This versatile application, accessible via various devices, ensures that data is captured accurately and conveniently. The system’s well-structured workflow simplifies the management of both outpatient (OP) and inpatient (IP) operations, ultimately leading to greater patient satisfaction. Moreover, its advanced EMR module is capable of capturing a wealth of data, granting easy and secure access to essential information. Utilizing a multi-tenant architecture, the system adeptly handles multiple locations or sites independently, establishing itself as a flexible option for healthcare organizations. This flexibility not only allows hospitals to tailor their services to meet specific needs but also guarantees consistent high-quality care across all facilities, thereby empowering healthcare providers to adapt to the evolving demands of patient care. As a result, hospitals can enhance their overall service delivery while maintaining efficiency and effectiveness.

What is HEKMA?

HEKMA stands at the forefront of innovation, leveraging artificial intelligence to improve the effectiveness of clinical trials through enhanced patient recruitment, evaluation of trial feasibility, and improved patient engagement. Their all-encompassing platform serves a wide range of stakeholders, including contract research organizations (CROs), pharmaceutical companies, healthcare providers, and patients, by combining electronic health records (EHRs) with AI-enhanced trial matching, clinical trial management systems, and patient engagement tools. HEKMA's primary objective is to reduce enrollment delays, increase access to clinical trials—particularly for marginalized groups—and streamline the clinical research workflow to create a process that is more efficient, transparent, and focused on patient requirements. With a unique combination of healthcare expertise, artificial intelligence technology, and clinical operations knowledge, HEKMA ensures compliance with essential industry standards, such as HIPAA, 21 CFR Part 11, GDPR, and HL7/FHIR, maintaining the highest levels of regulatory adherence. By embracing cutting-edge technology, HEKMA aspires to revolutionize the clinical trial landscape, ultimately driving progress in medical research and enhancing patient outcomes. Their commitment to innovation not only addresses current challenges in clinical research but also positions them as leaders in shaping the future of healthcare.

Media

Media

No images available

Integrations Supported

Additional information not provided

Integrations Supported

Additional information not provided

API Availability

Has API

API Availability

Has API

Pricing Information

Pricing not provided
Free Version
Free Trial Offered?

Pricing Information

Pricing not provided
Free Version
Free Trial Offered?

Supported Platforms

SaaS
Android
iPhone
iPad
Windows
Mac
On-Prem
Chromebook
Linux

Supported Platforms

SaaS
Android
iPhone
iPad
Windows
Mac
On-Prem
Chromebook
Linux

Customer Service / Support

Standard Support
24 Hour Support
Web-Based Support

Customer Service / Support

Standard Support
24 Hour Support
Web-Based Support

Training Options

Documentation Hub
Webinars
Online Training
On-Site Training

Training Options

Documentation Hub
Webinars
Online Training
On-Site Training

Company Facts

Organization Name

MEDAS

Company Location

United Arab Emirates

Company Website

www.medasuae.com

Company Facts

Organization Name

HEKMA

Date Founded

2018

Company Location

United States

Company Website

www.hekma.ai/

Categories and 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

Categories and 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

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