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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.

What is Antidote?

Antidote acts as a recruitment hub for clinical trials, accelerating the pace of medical research by linking patients with sponsors through specialized recruitment services and an intuitive matching search engine. To combat the issue where over 80% of clinical trials experience setbacks from a lack of participants, Antidote provides sponsors with a centralized, vendor-neutral dashboard that streamlines referrals from various sources, automates the outreach for due diligence and owner letters, and tracks enrollment and return on investment metrics in real time, while delivering valuable analytics on sites and candidates with updates every hour. For patients, Antidote’s smart matching system transforms complex inclusion and exclusion criteria into simple guided Q&A interactions, ultimately presenting them with current clinical trial listings and tailored notifications for new matching opportunities. The platform is built to support both bulk and individual record imports, complete with automated validations, and it boasts user-friendly, multilingual interfaces that are optimized for mobile devices. By simplifying the recruitment process, this innovative solution promotes more effective collaboration between researchers and potential participants, ultimately leading to improved outcomes in clinical studies. Moreover, Antidote’s commitment to accessibility ensures that a diverse range of patients can easily engage with clinical trials, thereby enriching the research landscape.

Media

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Media

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 Trial Offered?
Free Version

Pricing Information

Pricing not provided.
Free Trial Offered?
Free Version

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

HEKMA

Date Founded

2018

Company Location

United States

Company Website

www.hekma.ai/

Company Facts

Organization Name

Antidote

Date Founded

2010

Company Location

United States

Company Website

www.antidote.me/

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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