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Bioclinica offers the industry's only purpose-built, end-to-end, configurable randomization and trial supply management software platform. The flexible, intelligent RTSM platform combines the latest release of Bioclinica's IRT and advanced trial supply optimization and forecasting software to significantly cut time, effort and cost for even the most complex global trials.

Bioclinica Agile RTSM

Run and compare different supply scenarios against trial objectives (e.g. schedule, cost, feasibility) for the optimum supply strategy

Accurately assess drug demand at study and program level; provide finished goods to API

Build, implement, test and deploy protocols in as little as two weeks with an integrated supply strategy

Accomplish fast, accurate patient randomization aligned with protocol

Get the right drugs to the right sites and patients at the right time with integrated, optimized RTSM

Identify and adjust enrollment and supply needs based on actuals

Reduce waste and destruction and reconciliation time, effort and cost with continually updated supply plans

Achieve faster database lock, lower cost and effort, yet higher quality data with continual optimization

Unified Medical Imaging, EDC & IRT

When medical imaging, electronic data collection and recruitment and randomization are managed separately, clinical trials are burdened by duplicate data entry, excessive time resolving enquiries and manual reconciliation between systems. Bioclinica's best-in-class integration of medical imaging, EDC and IRT bridges critical aspects in the clinical trial to enable the collection, visibility and management of Bioclinica Medical Imaging, Bioclinica EDC and Bioclinica IRT data and to achieve a harmonious workflow – through a single dashboard.

IRT ↔ EDC
Accelerate your clinical trial with quality data and benefit from:

  • Proactive visit-based requests for missing images
  • No delays with monthly logs
  • No manual reviews/reconciliation and updates
  • No data management loads, edit checks, and data diagnostics
  • Imaging visit dates that facilitate site communications for outstanding data
  • Clear view of subject status and subsequent imaging visits

IRT ↔ Imaging
Gain efficiencies in patient recruitment and management and benefit from:

  • Real-time notification of cases
  • Immediate projection of the protocol visit schedule
  • Auto creation of screening records and subject visit records
  • No delays with monthly logs
  • No manual reviews/reconciliation and updates
  • Adherence to CDISC standards

Unified Medical Imaging, EDC & IRT

Bioclinica's integration of these systems unifies key processes, creating opportunities to improve the experience of patients and sites alike.

DOWNLOAD OVERVIEW SHEET

See Bioclinica's agile approach to IRT development…

With Bioclinica's Agile RTSM platform, our customers are building, implementing, testing and deploying new protocols in as little as two weeks, reducing drug waste and study costs by millions of dollars and identifying changing trial conditions months in advance, lowering the risk to patients and studies.

MANAGING CLINICAL SUPPLY CHAIN RISKS WITH THE RIGHT RTSM PLUS TRIAL SUPPLY OPTIMIZATION

INTERACTIVE RESPONSE TECHNOLOGY (IRT)

The leading end-to-end product and technology solution for sponsors and CROs.
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TRIAL SUPPLY OPTIMIZATION

Powerful forecasting and demand-planning technology to manage global logistics of the clinical supply chain.
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ADDITIONAL RESOURCES

CAREFUL CONSIDERATION OF RTSM CHARACTERISTICS CAN MITIGATE CLINICAL SUPPLY CHAIN RISKS

Download White Paper

GETTING TRUE TO AGILE IRT: 5 QUESTIONS TO ASK YOUR IRT VENDOR

Download White Paper

MANAGING CLINICAL SUPPLY CHAIN RISKS WITH THE RIGHT RTSM + TRIAL SUPPLY OPTIMIZATION

Download Infographic

Feasibility of Shipping Clinical Trial Drugs Directly to Patients' Homes

Download Case Study

Leader in Clinical Trial
Management Solutions

Successful clinical trials require the ability to see key details and uncover hidden insights. Bioclinica utilizes science and technology to bring clarity to clinical trials, helping companies to develop new life-improving therapies more efficiently and safely.

Dr Joby John chairing a panel discussion tomorrow 8am at #DIA2019 on ways to improve connectedness of clinical data… https://t.co/BPzi1geKsv
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We’re at #DIA2019. Visit us at booth #1831 to learn more about our rapidly growing services and meet face to face… https://t.co/rK7V1Aclov
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Learn about When EDC is not enough: Automating multi-country data collection and complete workflows at #DIA2019! Ja… https://t.co/zJfytNpz82
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In San Diego for #DIA2019? Visit us at booth #1831 and meet face to face with our team to learn more about our rapi… https://t.co/T4U4oNXlxo
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