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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 Biorce Aika?

Biorce's Aika is an innovative AI-powered clinical intelligence platform that revolutionizes the clinical trial lifecycle by converting labor-intensive processes for protocol creation and feasibility assessments into streamlined, evidence-based automation. Drawing on insights from nearly one million real-world trials, Aika can rapidly generate initial study protocols, detailed regulatory documents, site feasibility assessments, risk management plans, and other essential components of trials much quicker than traditional methods, thus reducing the likelihood of delays and costly revisions. This platform promotes complete transparency in its recommendation processes, empowering teams to confidently convey their decisions to regulatory bodies while ensuring expert supervision remains intact. Furthermore, Aika effectively marries the rapid efficiency of AI with deep clinical expertise, significantly shortening trial preparation durations from weeks to just days, which minimizes amendment risks and overall project vulnerabilities. By integrating seamlessly into current workflows without necessitating extensive retraining, Aika allows clinical trial teams to prioritize strategic decision-making over tedious administrative responsibilities. As a result, the focus shifts towards enhancing trial outcomes and optimizing resource allocation, ultimately driving innovation in clinical research practices.

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

Biorce

Date Founded

2024

Company Location

Spain

Company Website

www.biorce.com/our-software

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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