Patient Recruitment/Retention Services & Products
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Ergomed's Patient-Centric Focus Drives Our Team
2/6/2025
Ergomed places patients and their care partners’ needs at the core of our services. We strive to build empathetic relationships with patients and their care partners, not just during the trial but also before and after. Our team provides personalized support, aiming to alleviate the burden of study participation. Ergomed and our trusted partners are deeply committed to bringing lifesaving treatments to patients.
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Integrated Trial Services
11/22/2024
We work as a single provider to empower patient and site participation in clinical trials. Our Integrated Trial Services team is dedicated to creating partnerships with our Sponsor and CRO clients, building strategic and unique combinations of solutions to accelerate trial timelines.
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Home Trial Support
11/22/2024
By removing barriers, and bringing trials to patients where they live, we can expand the geographical reach of clinical research across the globe allowing more patients to participate. Our patient-centric delivery means we can create convenience and comfort working the schedule of the trial around the schedule of the patient and their family, not the other way around. This approach provides important access to medical care, enhances the inclusivity of clinical trials and advances drug development for all.
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Patient Support And Commercial Services
8/29/2024
Global solutions tailored for your unique needs.
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ConneX
2/25/2019
ConneX is a global travel solution providing in-market services and support, designed to meet the unique travel needs of each study, whether it be for rare disease, diverse populations, pediatrics, etc. Our offering removes the burden of complex travel arrangement from site staff, while peace of mind is established for participants, their families and caregivers.
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Clinical Operations
3/4/2016
Clinical operations are a critical component in all studies. SynteractHCR’s highly skilled staff is well-versed in clinical trial operations including implementing, monitoring and managing the clinical components of a study. From start-up to close-out, experienced clinical managers and clinical research associates (CRAs) oversee each study’s clinical processes to ensure proper planning, conduct, patient safety, and data quality, while fostering good communication between study sites and sponsor.
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Phase I-IIA Clinical Trials
5/29/2013
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.
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Oncology Clinical Trials
5/29/2013
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.
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Phase IIb-III Clinical Trials
5/29/2013
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.
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Patient Recruitment/Retention
5/29/2013
INC Research/inVentiv Health's experienced team of specialists can help you find the right patients and the right sites to support smooth completion of your global trials.