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Medical Imaging

Your trial needs experts who can see more deeply into essential imaging data and uncover clues and evidence others might miss.

Areas of Expertise

ONCOLOGY

Experience across 1100+ oncology imaging trials
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NEUROSCIENCE

Unequalled expertise advancing CNS trials with imaging endpoints
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MUSKULOSKELETAL (MSK)

Proven support for studies with MSK imaging endpoints
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CARDIOVASCULAR

Expert Imaging support for Cardiovascular studies
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Additional Therapeutic Areas

Global experience supporting a broad range of indications
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EXPERT REGULATORY GUIDANCE

Unmatched expertise working with global regulatory agencies
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The deep experience you need

Bioclinica is the worldwide leader in medical imaging core lab services — providing life-science companies with clinical trial support for all phases and across all major indications. Our commitment to service and scientific excellence is focused on advancing our clients' drug development process.
Our therapeutically aligned team delivers operational expertise necessary to successfully design and manage your clinical trials with best-in-class operations, centralized image assessments, and global data management. We work together with sponsors and sites to capture and skillfully analyze imaging endpoints and deliver the highest quality data for your eligibility, safety, and efficacy studies.
Bioclinica provides global support for clinical trials through the use of SMART, a full suite of medical imaging services backed by proprietary, leading-edge technology. Bioclinica's SMART digital customer portal allows sites and sponsors to benefit from real-time access to their trial data for quicker go/no go decisions.

Bioclinica SMART

Our Digital Customer Portal Allows Sites and Sponsors to Benefit from Real-Time Access to Their Trial Data for Quicker Go/No Go Decisions.

Electronically upload imaging data from clinical trial sites via a web portal. Medical images are blinded and undergo rigorous quality checks to ensure the highest quality imaging data and maximize clinical trial efficiency. Sites can easily track and manage images through our custom designed submission portal.
Tracks all patients enrolled on studies and all imaging data generated during the course of a clinical trial. Qualified technicians use innovative tools to review, update, and assure compliance with clinical trial protocols and defined reading paradigms. Enables queries to be issued, tracked, and resolved.
High quality independent image review by in-house and contracted radiologists and therapeutic area imaging specialists. Bioclinica has developed and validated a library of image processing algorithms across therapeutic areas for qualitative and quantitative clinical trial endpoints. Independent review applications are configurable to meet client specifications.
A comprehensive reporting service for sites and sponsors which supports the management and review of data for clinical trials. Sponsors gain access to metrics reports, custom client reports, analysis results reports, safety and eligibility reports and billing reports.
Tools that enable clinical trial data delivery, including patient data and imaging data, to sponsors, external vendors and partners. Bioclinica's transfer tools support a wide range of formats, to meet client and project specifications.

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Leader in Clinical Trial
Management Solutions

Bioclinica is organized into three business segments so that we can provide expert service and multifaceted technologies. Our Medical Imaging & Biomarkers segment includes an Imaging Core Lab, a Cardiovascular Safety division, and a Molecular Marker Laboratory. Our eHealth segment comprises eClinical Solutions, Randomization & Trial Supply Management, Safety & Regulatory Solutions, and Financial Lifecycle Solutions. Under the Global Clinical Research segment, we offer a network of research sites, patient recruitment, and a Post-Approval Research division.

Our Medical Imaging team is in the spotlight for a job well done! https://t.co/fkmt0zvPhf https://t.co/D7YMTeiSd3
bioclinica (2 days ago)
RT @melfass: "What this agreement means is that we can allocate scarce resources to areas of higher risk" @US_FDA on MRA with @EMA_News at…
bioclinica (3 days ago)
RT @DrugInfoAssn: What has been the biggest takeway for your organization so far? Tweet @ us using #DIA2017
bioclinica (5 days ago)
"Q" on #RBM & Total Quality Mgmt? @Kristin_Mauri has "A" @DrugInfoAssn #DIA2017 https://t.co/MqCxkmAfa0
bioclinica (5 days ago)
Kristen Mauri shows the @DIA audience the value of risk based monitoring https://t.co/ssJCfc9gQ5
bioclinica (5 days ago)
Innovation Theater Kristin Mauri of @bioclinica presenting on RBM & TQM @DrugInfoAssn #DIA2017 https://t.co/zsGroQcpiU
bioclinica (5 days ago)

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