Project Management Services & Products

  1. Medical & Regulatory Affairs

    Taking new products successfully through clinical development, submission and approval can be a difficult, expensive and lengthy process. SynteractHCR’s medical regulatory affairs group offers a wide range of services that spans the full range of product development, including training, performed by senior regulatory professionals with experience in pharmaceutical, diagnostic, device and biotechnology industries. Our medical regulatory affairs team is here to deliver on aggressive timelines and control costs, while ensuring compliance and patient safety.

  2. Strategic Resourcing Functional Services

    Our dedicated functional teams have the experience to be your partner in clinical research. We deliver a variety of clinical development services customized to fit your objectives, whether you need a single function across several drug programs, a range of functions within a single therapeutic area, a complete staff lift-out or any other defined need.

  3. 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.

  4. Oncology Clinical Trials

    The unique patient populations, study design challenges, and special endpoints associated with oncology trials demand specialized knowledge.  INC Research/inVentiv Health's Oncology team is uniquely qualified to manage that complexity.

  5. Phase IIb-III Clinical Trials

    With decades of experience in clinical trial design, INC Research/inVentiv Health offers a full range of clinical trial services including bioanalysis, biostatistics, data management, feasibility studies, global safety and pharmacovigilance, medical writing, project management, protocol and case report form design, quality assurance, regulatory affairs, risk management, site management, strategic planning, and study monitoring.

  6. Central Laboratory Solutions

    Remember the time when laboratory kits were ordered and reordered by sites faxing in pieces of paper, and laboratory reports were faxed and express mailed to investigative sites around the world? Sadly that time is still here for many central laboratory providers.

  7. DATATRAK Clinical and Consulting Services (DCCS)

    We deliver superior service through our DATATRAK ONE® program by aligning our service delivery processes and our integrated technology.

  8. eCOA Project Management

    Our great eCOA (electronic Clinical Outcome Assessment) Project Managers are responsible for successful and efficient delivery of every project and they also take responsibility for your diary’s design to ensure it meets all your protocol’s objectives while maximizing patient usability.

  9. Strategic Clinical Project Outsourcing

    RDP Clinical specializes in building highly experienced project monitoring teams that are a custom fit for your specific study demands/ needs that are geographically positioned in direct proportion to the site locations to maximize efficiency. 

  10. Clinical Project Management

    Marken’s intensive project management approach means that your project moves seamlessly through the clinical trial process.