Products and Services

  1. ERT Imaging

    Imaging technology that delivers results without the typical human bias.

  2. Phase I-IIA Clinical Trials

    INC Research/inVentiv Health conducts Phase I-IIa clinical trials quickly and efficiently at its dedicated 22,000 square foot clinical facility comprising more than 200 beds in four independent units. An extensive database and relationships with leading hospitals ensures rapid recruitment of study participants for a wide variety of trials.

  3. Patient Recruitment & Retention

    Bioclinica’s Patient Recruitment & Retention division enables companies to effectively recruit, engage, and retain patients for clinical trials in a timely and cost-effective manner.  We maintain an extensive patient database as well as patient communities that can be tapped for quality patients, provide customized marketing programs to aid recruitment, develop best-in-class retention materials, and offer an array of tools and services to drive site performance.

  4. Late Stage Clinical Research Services

    In today’s competitive landscape, getting a drug on the market is no longer about meeting clinical trial requirements, receiving regulatory approval and launching the drug. Drug developers need to generate evidence that shows whether a drug works in the real world and the benefit and value it provides to the healthcare system and patient.

  5. Medidata RBM

    Medidata RBM is Medidata’s risk-based monitoring application (RBM) that allows you to design and conduct any RBM program.

    • Configurable. Efficiently and compliantly reduce the amount of source document verification (SDV) conducted to any level you decide.  Medidata RBM applies cloud technology and strategic consulting services to ensure study-, site- and patient-level risks are assessed upfront and monitored centrally so issues that arise during the study are easily detected.
    • Integrated EDC. Configurable integration with Medidata’s EDC system eliminates the need for engineering or technical expertise.
    • Agile. Configured for your study’s specific data and risks, so you can select key risk indicators (KRIs) that are right for your study and use thresholds that adjust automatically as the study is ongoing.
  6. Mobile eClinical Software: mSource

    mSource is Medrio's mobile eSource application that includes mPRO, mCapture, and mConsent. All products are native applications and are designed for use in early phase and Phase I research.

  7. Pharmaceutical Contract Packaging: Primary And Secondary Packaging Services

    Ropack Pharma Solutions offers turnkey contract primary and secondary pharmaceutical packaging services of solid oral dosages. Whether in blisters, bottles, flip-top vials, stick-packs, sachets or strip-packs, we manufacture and package powders, tablets and capsules for clinical or commercial applications.

  8. Contract Packaging Services for Specialty Pharmaceutical Products

    Primary Packaging
    PCI features primary packaging of oral solids and powders for specialty products including thermoform and cold form blistering, pouching, bottling, and tube filling. Packaging suites support ISO 8 / Class 100,000 clean room requirements.

  9. Electronic Regulatory & Study Binders

    All clinical trials collect regulatory documentation in order to receive authorization to conduct the trial at investigative sites. Trials require a Regulatory Binder and many keep separate Study Binders.

  10. Risk Management & Pharmacovigilance

    Led by industry safety expert, Annette Stemhagen, DrPH, FISPE, UBC’s Risk Management, Registries & Epidemiology team brings unmatched passion and commitment to your product and your reputation.