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Strategic Partnership with Third-Party Vendors

Every successful clinical project begins with a clear vision, strategy, and plan that can be achieved.

Our partnership with third-party vendors aims to pool resources and deliver the best clinical trial outcomes in the biotech and pharmaceutical industries. At Zanteris, our partners remain independent, and we also work together to build successful on-budget projects and on-time trials.

Value Behind Strategic Partnership with Third-Party Vendors

As a functional CRO in Clinical Operations, we offer preferred partners to work with and to support the deliverable of your clinical trial.

DCT Solutions (eCOA, telemedicine, and survey)

Our partners ensure that participants can easily go through research that may seem burdensome under certain trial constructs. In most cases, DCT solutions help improve patient engagement.

Medical and Central Imaging

Our partnership with Medical and Central Imaging providers helps find diseases in their early stages during clinical trials. This partnership gives pharma and biotech industries the ability to get better patient outcomes. The various types of available medical and central imaging include Magnetic Resonance Imaging (MRI), Positron Emission Tomography (PET), and Computed Tomography (CT).

Data Management

In data management via eCRF and medical coding, our partners can generate high-quality and statistically sound data. It also helps in saving time during the process of “drug development to marketing.”

Biostats

With the help of our biostatistics partner, we can prevent fraud and unintentional errors during clinical trials. Most times, frauds occur due to data fabrication, and we work to avoid all forms of falsification.

Patient Engagement Services

Our partner in patient engagement services helps with home nursing, concierge, payments, and travel. With patient engagement, we can ensure participants have positive behaviors, including helping with their health and care to improve health outcomes.

eTMF, ISF

With our eTMF partner, we can utilize systems and server applications to manage the various stages of clinical trials. With eTMF, we can effectively guide, store, and track long documents and data relating to the trials.

ISF contains essential documents that show the clinical trial site and investigators adhere to regulatory requirements by the ICH GCP guidelines.

Staff Resourcing

Our Staff Resourcing partner helps to ensure we have the best staff working on medical research or clinical trials. We prioritize staff recruitment and retention to ensure better comprehension of processes needed in various clinical trials or studies.

OUR SERVICES GUIDE

What it’s like working with us

… a good sense of what it takes to successfully navigate challenging clinical trials to achieve success on behalf of his customers. In particular, his data and information expertise gave him the ability to mentor, support and coach teams towards a more data driven approach to strategy and outcomes. …

Senior Vice President
Clinical Informatics
Global CRO

Project Manager Resourcing

Clinical Project Management Resourcing

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Program & Portfolio

Clinical Operations Consulting

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Team Development

Human Efficiency Consulting

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