List of Acceliant eClinical Suite Customers
Santa Clara, 95054, CA,
United States
Since 2010, our global team of researchers has been studying Acceliant eClinical Suite customers around the world, aggregating massive amounts of data points that form the basis of our forecast assumptions and perhaps the rise and fall of certain vendors and their products on a quarterly basis.
Each quarter our research team identifies companies that have purchased Acceliant eClinical Suite for Clinical Trial Management from public (Press Releases, Customer References, Testimonials, Case Studies and Success Stories) and proprietary sources, including the customer size, industry, location, implementation status, partner involvement, LOB Key Stakeholders and related IT decision-makers contact details.
Companies using Acceliant eClinical Suite for Clinical Trial Management include: PPD, a United States based Professional Services organisation with 40000 employees and revenues of $4.70 billion, Lupin Limited, a India based Life Sciences organisation with 24006 employees and revenues of $2.55 billion, Cliantha Research Partners, a United States based Life Sciences organisation with 1000 employees and revenues of $400.0 million and many others.
Contact us if you need a completed and verified list of companies using Acceliant eClinical Suite, including the breakdown by industry (21 Verticals), Geography (Region, Country, State, City), Company Size (Revenue, Employees, Asset) and related IT Decision Makers, Key Stakeholders, business and technology executives responsible for the ERP Services and Operations software purchases.
The Acceliant eClinical Suite customer wins are being incorporated in our Enterprise Applications Buyer Insight and Technographics Customer Database which has over 100 data fields that detail company usage of ERP Services and Operations software systems and their digital transformation initiatives. Apps Run The World wants to become your No. 1 technographic data source!
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| Logo | Customer | Industry | Empl. | Revenue | Country | Vendor | Application | Category | When | SI | Insight |
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Cliantha Research Partners | Life Sciences | 1000 | $400M | United States | Acceliant | Acceliant eClinical Suite | Clinical Trial Management | 2013 | n/a |
In 2013, Cliantha Research Partners implemented Acceliant eClinical Suite as its Clinical Trial Management application to support clinical operations and biometrics. The deployment anchored Acceliant eClinical Suite across study setup and ongoing data management workflows, positioning the platform as the primary system for electronic data capture and patient reported outcomes within Cliantha's clinical teams.
The implementation leveraged the suite's integrated EDC-ePRO components and built-in mobility to enable remote data capture and real time access to study data. Configuration work focused on study build, eCRF configuration, query management and role based access for data management and biometrics, reflecting capabilities typical of Clinical Trial Management platforms.
Operationally the Acceliant eClinical Suite was rolled into Cliantha's clinical operations and biometrics groups, providing a unified interface for investigators, data managers and biometricians to manage study data. The deployment emphasized mobile enabled data entry and workflow automation to reduce manual handoffs and support distributed data management practices.
Cliantha's Associate Director of Biometrics stated the solution was selected for its user friendly design and process oriented architecture that drives efficiency, lowers costs and accelerates clinical trial studies, and Acceliant's CTO described the platform as an integrated EDC-ePRO solution with mobility that allows data management from anywhere, anytime. Governance adjustments centered on standardizing data management workflows and aligning operational processes to the capabilities of the Acceliant eClinical Suite.
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Lupin Limited | Life Sciences | 24006 | $2.5B | India | Acceliant | Acceliant eClinical Suite | Clinical Trial Management | 2017 | n/a |
In 2017, Lupin Limited implemented Acceliant eClinical Suite for BA/BE studies, selecting the platform to address a need for a robust, user friendly and cost effective clinical operations system. The engagement targeted Clinical Trial Management for bioavailability and bioequivalence trials and aimed to move control of clinical technology back in house because Lupin had been outsourcing their current technology and wanted an easy to use platform for the internal team.
Implementation centered on study setup, configurable protocol workflows, and document management to remove the previous need to manage multiple discrete tools per trial. Acceliant eClinical Suite was configured to allow independent trial creation by clinical operations staff, to capture specific workflows such as blood sample collection time entry, and to centralize structured data collection and review processes consistent with Clinical Trial Management functionality.
The deployment emphasized a feature rich configuration model that removed per trial constraints by providing unlimited pages, sites, and subjects and a licensing allowance of 100 trials per year, delivering a predictable and consolidated cost structure. Operational scope focused on Lupin's BA/BE study teams and internal clinical operations, with Acceliant eClinical Suite providing Clinical Trial Management capabilities across study design, participant tracking, and document control.
Governance was adjusted toward decentralized provisioning and standardized workflows so study teams could provision trials and manage documents without individual trial pricing negotiations. Acceliant eClinical Suite now serves as Lupin Limited's centralized Clinical Trial Management platform for BA/BE studies, addressing prior tool fragmentation while enabling configurable data capture and review workflows.
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PPD | Professional Services | 40000 | $4.7B | United States | Acceliant | Acceliant eClinical Suite | Clinical Trial Management | 2007 | n/a |
In 2007, PPD implemented Acceliant eClinical Suite for Clinical Trial Management. The Acceliant eClinical Suite was used alongside Excel and SAS output to perform data listing reviews and validation in accordance with Good Clinical Practices and PPD Global Standard Operating Procedures.
Implementation focused on operationalizing clinical data review and validation workflows within the Clinical Trial Management environment, aligning the application with PPD data management and biostatistics groups to support listing generation, review reconciliation, and documented audit trails. Integrations were explicitly configured to consume SAS output and to export review artifacts into Excel for manual reconciliation, while standard Clinical Trial Management capabilities such as study and subject tracking, configurable review workflows, and controlled signoff were leveraged to enforce GCP and SOP controls. Governance centered on embedding SOP-aligned validation steps and formal review signoff into the Acceliant eClinical Suite workflow to ensure compliant data listing reviews and validation.
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Buyer Intent: Companies Evaluating Acceliant eClinical Suite
- BPR Hub India, a India based Professional Services organization with 15 Employees
Discover Software Buyers actively Evaluating Enterprise Applications
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