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Fast track your study!


  • Uniform cost model

  • Study wizard for setup

  • Agnostic smart device integration

  • Scalable and cost-effective for
    any size trial

AcquisCT  Clinical Trial


Transforming Global Clinical Trials

Scalable, fast, and cost effective for any size trial, AcquisCT, the clinical trial software on the AcquisHEALTH platform encourages research for all consultants, researchers and clinicians.

Decentralized clinical trials (DCTs) can improve patient access to research, reduce costs, and speed up the development of new treatments. 


AcquisCT includes robust data security and privacy protections. It is carefully designed to provide reliable and practical support for DCTs since they collect sensitive data, including medical records, genomic data, and patient-reported outcomes. The platform securely stores these data to ensure unauthorized individuals do not access it. For example, DCTs require new ways to collect and manage data, monitor patients, and communicate with investigators and researchers.


AcquisCT complies with the regulatory frameworks for US and EU clinical trials. It addresses the new challenges of DCTs, such as how to ensure that patients are appropriately informed about the risks and benefits of participating and how to remotely monitor patients for adverse events. 


We are revolutionizing the way clinical trials are conducted. By making them more convenient and accessible for patients, DCTs can increase participation rates and improve the quality of data collected. This can lead to faster development of new treatments, making the most of research funds, and providing better health outcomes for all.

Case Study:
The OATS-I project

Many clinical trial cloud solutions have come to market to support global and decentralized clinical trials, but are cost-prohibitive and focused on big pharma drug delivery trials. Not every study needs al that.


Here's how we delivered the perfect solution for the OATS-i project

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View the case study >

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AcquisCT is designed so that you can start and run your study without us. Built in wizards help you design, test and run your study as quickly and easily as possible.


Easily manage and monitor your multi-site study with real-time data visibility and detect issues as they are reported in the system, such as increased study attrition or recruitment level tracking across sites for the best patient engagement and program compliance results.

AcquisCT: Unparalleled Features and Benefits:

  • Flexible, Low-Cost Pricing Model with no hidden costs. AcquisCT includes hosting, study setup support, ongoing support, onboarding users, and study participants in Observational Trials, Randomized Control Trials, Medical Device Certifications, and New Drug Trials. Everything needed with a straightforward price.

  • Seamless interoperability Data can be imported automatically from (standards-compliant) EHRs, reducing time and costs while improving data quality and efficiency. Built upon the FHIR standard and supports coding systems like ICD-10 and SNOMED.

  • Integrated Patient Portal with no borders. Decentralized trials require that participants can submit data to a study from wherever they are. Researchers capture participant data (eConsent, Study Questionnaires), upload biomedical sensor and wearable device data, and report adverse events as part of electronic patient-reported outcomes (ePRO's) - anywhere. The patient portal also allows for that data to be returned to the participant at the end of a study.

  • Built-in encryption by default – we take security very seriously. AcquisCT utilizes a novel multi-level encryption approach to ensure that a patient’s identity and medical data are fully anonymized and uniquely secured to comply with global and national data security standards such as GDPR and HIPAA. Other companies charge for encryption as an added extra. It comes standard with AcquisHEALTH Platform products.

  • Easy-to-use Study Creation Wizard.
    Study teams can easily create and manage research studies using the intuitive study setup wizard within the AcquisCT environment.

    Researchers can separate the study into stages (Baseline, Visit 1, Visit 2), set up and capture multiple data types using the questionnaire wizard, and collaborate with others to validate the setup before recruiting study participants.

  • Standard & Custom Questionnaires. Researchers can use easy pre-built standard questionnaires or easily create customized questionnaires utilizing the drag-and-drop questionnaire wizard.

  • Personalized Patient Dashboards. Researchers can customize each study participant or group of participants' dashboards using the AcquisHealth CT Drag-and-Drop Dashboard Wizard.

  • Comprehensive Electronic Data Capture The (EDC) system allows the capture and secure storage of all data for your research studies.

  • Administrative Study Management Interface.
    View and manage all the studies within your organization, department, or division, including documents (ethics/consent), roles, and access, as well as audit and other regulatory and clinical requirements such as ICH-GCP or 21 CFR Part 11.

  • Secure In-App Messaging. Researchers and patients can securely communicate via an internal messaging service, ensuring all study data is captured in a single place, avoiding potential email security issues.

  • Support for key research features
    such as document storage (adverse outcomes, consent forms, imaging) and data export for use in other platforms, such as statistical packages. Researchers can export all data for use in external statistical analysis software packages such as SAS/STATA/SPSS. Previously developed analysis algorithms can also be integrated into the study using the calculated fields feature. 

  • ​​Unique Data Security.
    Multi-Level data encryption ensures maximum data security and data anonymization as standard to meet GDPR and HIPAA compliance requirements.

  • Built in API support
    to extract data from EHR to EDC with data reusability (FHIR/CDISC Mapping). Select data can be back to the patient via Patient Portal.

  • Centralized Data Management.
    All research study data is stored securely in one place using the AcquisCT environment. Seamlessly integrate Data from eHRs, eCRFs, ePROs, LIMS, biomedical sensors, and wearables. A single shared patient record at the platform's core means a single unified view of patients' medical and research data is possible with AcquisHEALTH.

  • Data Validation 
    By ensuring data is validated as it’s entered, data efficiency, accuracy and quality are assured with the possibility of  source data verification.

Roadblocks From the Research Lab to Clinical Practice


Health research can be full of promise and potential - until the reality of cost hits. Healthcare funding for research studies is highly competitive, only sometimes available, and requires tremendous organization up front just to apply. Stumbling blocks like this are stopping progress for people that need it. Challenges voiced by researchers, students and clinicians include:


  • Missed opportunities to manage and collaborate on studies across research organizations with collaborative administrative, compliance, ethical, and regulatory tools.

  • Clinical trial software is prohibitively expensive for non-pharma organizations.

  • Electronic Data Capture (EDC) in non-clinical and non-compliant environments (Word, Excel, and Google Docs, for example) introduces data security and data quality risks that result in corruption and loss.

  • Sensor integration and decentralized trial solutions have opened an avenue for research via decentralized trials, but require significant investment. We can leverage these data sources today for real-time analysis now.

  • A patient cannot typically re-use study data as part of their regular care. A test ordered for a study can now be added to the patient's record, saving crucial time and costs to the patient and their providers.

How AcquisCT is Translating Innovative Research into Clinical Practice Now


Funds go further with affordable integrated solutions focusing on research instead of technology implementation. Clinical trial software can be based on shared costs and shared services and use existing working technologies in any size organization. The CT Platform bypasses difficulties by:

  • Securing shared clinical data in clinically compliant environments with tools like eCRF, ePRO, and eConsent using decentralized, globalized, and internationalized features that maximize and speed up research outcomes
    to get to clinicians faster.


  • Provision of a secure, single, properly accessed repository
    for all research data, management, and administration.


  • Integration of sensor and device data in real-time enables further, faster innovation in predictive analysis.

  • Decentralization and distribution of trial solutions with a tailored Patient Portal (ePRO) that empowers patients to securely share their trial data with their primary care providers for their benefit while reducing redundancy and pressure
    on healthcare services
    for assessments already run and carried out by trials. 

AcquisCT solves real challenges today

for better, faster progress through research.

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