We Are Redefining Clinical Trials
With Inclusivity And Innovation

Partner with TruVision

We utilize a holistic approach in the execution of both traditional and decentralized clinical trials.

Inclusive Patient Recruitment Strategies

Focused efforts to recruit participants from historically underrepresented populations.

Regulatory Compliance

TVCRP's adherence to ISO 14155:2020 standards ensures high quality clinical trial practices and participant safety.

Integrated Clinical Navigators

Use of highly trained clinical navigators providing "high touch"throughout the clinical trial to build trust, ensure patient comfort and to retain patients in the trial until its completion.

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Enhances Accessibility

Our flexible approach to clinical trials allows participants options of participation that fit a persons day to day life, removing geographic barriers, and mitigating some of the impediments of social determinants.

Advanced Technology Integration

Use of Ai powered monitoring systems and telehealth visits to enhance patient engagement, patient trust, and data accuracy.

Improved Data Accuracy

Ai powered monitoring systems provide real time insights into patient behavior, reducing errors and increasing trial efficiency.

Flexible Clinical
Trial Execution

We manage clinical trials in the investigators office, mobile clinical settings, non-traditional sites, and in a patient's home.

Screenshot

Inclusive Patient Recruitment Strategies

Focused efforts to recruit participants from historically underrepresented populations.

Improved Data Accuracy

Ai powered monitoring systems provide real time insights into patient behavior, reducing errors and increasing trial efficiency.

Integrated Clinical Navigators

Use of highly trained clinical navigators providing "high touch"throughout the clinical trial to build trust, ensure patient comfort and to retain patients in the trial until its completion.

Regulatory Compliance

TVCRP's adherence to ISO 14155:2020 standards ensures high quality clinical trial practices and participant safety.

Flexible Clinical
Trial Execution

We manage clinical trials in the investigators office, mobile clinical settings, non-traditional sites, and in a patient's home.

Advanced Technology Integration

Use of Ai powered monitoring systems and telehealth visits to enhance patient engagement, patient trust, and data accuracy.

Enhances Accessibility

Our flexible approach to clinical trials allows participants options of participation that fit a persons day to day life, removing geographic barriers, and mitigating some of the impediments of social determinants.

Minimize Financial Liability with Reliable Results

TruVision Clinical Research Partners provides clear information about pricing and the return on investment (ROI) that sponsors can expect with a focus on the cost implications of under performing clinical trials and low diversity enrollment.

Transparent Pricing

The cost structure is based on the scope and complexity of the clinical trial including factors such disease prevalence, number of participants, duration of the trial, complexity of of the clinical trial (CT) procedures, device versus a drug study and level of clinical navigator involvement. Utilizing our DCT model, TVCRP can reduce the overhead costs associated with the traditional CT model.

Sponsor ROI

The return on investment is significantly enhanced by addressing 2 critical issues: the high cost of failed trials and the impact of absent or low recruitment of historically underrepresented groups. Failed clinical trials can cost a Sponsor millions of dollars, often due to inadequate patient recruitment, poor data quality and lack of participant diversity. Low diversity leads to less generalizable data, ineffective treatments for certain subpopulations and potential regulatory setbacks.

Cost of Failed Trials

TVCRP's model reduces the risk of CT failure by improving patient recruitment and retention through inclusive strategies and comprehensive patient support. The use of Ai-powered monitoring systems ensures high-quality data collection, reducing errors and  Increasing trial efficiency. This approach minimizes the likelihood of trial failure, creating significant cost savings associated with restarting or redesigning a trial.

Effective Clinical Trial Enrollment

By utilizing an aggressive, inclusive approach in historically underrepresented communities CVCR ensures that clinical trial data is more representative of the general population. This diversity in participants leads to more accurate and generalizable findings, improving the chances of regulatory approval and market success.

TruVision Clinical Research Partners has a team of highly experienced senior nurses staff called clinical navigators. Our team of experienced clinical navigators provide on going patient support throughout a trial to its conclusion. TVCRP navigators are keenly focused on social determinants of health (SODH) and will actively work to mitigate the impacts. Our navigators will be made available to your institution to ensure that you have the support necessary to successfully conduct your studies.

TruVision Clinical Research ICONS (112 x 113 px) (2)
  • Implementation

    The implementation process includes detailed planning and coordination with the clinical trial team, including site selection, patient recruitment, and training for local healthcare providers. 

  • Training & Certification

    When necessary TVCRP provides GCP training and certification.

  • Support Services

    Continuous support is provided to the PI and patient throughout the trial, including (if necessary) personalized in-home visits, telehealth consultations, and real-time monitoring of patients performing CT tasks.

TruVision Clinical Research Partners has a team of highly experienced senior nurses staff called clinical navigators. Our team of experienced clinical navigators provide on going patient support throughout a trial to its conclusion. TVCRP navigators are keenly focused on social determinants of health (SODH) and will actively work to mitigate the impacts. Our navigators will be made available to your institution to ensure that you have the support necessary to successfully conduct your studies.

TruVision Clinical Research ICONS (112 x 113 px) (2)
  • Implementation

    The implementation process includes detailed planning and coordination with the clinical trial team, including site selection, patient recruitment, and training for local healthcare providers. 

  • Training & Certification

    When necessary TVCRP provides GCP training and certification.

  • Support Services

    Continuous support is provided to the patient throughout the trial, including (if necessary) personalized in-home visits, telehealth consultations, and real-time monitoring of patients performing CT tasks.

PATIENT SUPPORT

TVCRP provides comprehensive support services to enhance the likelihood of the success of clinical trials in all domains.

  • Telehealth

    Telehealth enhances patient engagement and data accuracy.

  • Support Services

    Continuous support is provided to the patients throughout the trial, including (if necessary) personalized in-home visits, telehealth consultations, and real-time monitoring of patients performing CT tasks.

  • Patient Support

    TVCRP has access to a Patient Care Center that is the
    central hub for remote monitoring of the CT process.

  • Telehealth

    Telehealth enhances patient engagement and data accuracy.

  • Support Services

    Continuous support is provided to the patients throughout the trial, including (if necessary) personalized in-home visits, telehealth consultations, and real-time monitoring of patients performing CT tasks.

  • Patient Support

    TVCRP has access to a Patient Care Center that is the
    central hub for remote monitoring of the CT process.

TruVision Clinical Research ICONS (112 x 113 px) (1)
  • Telehealth

    Telehealth enhances patient engagement and data accuracy.

  • Support Services

    Continuous support is provided to the patients throughout the trial, including (if necessary) personalized in-home visits, telehealth consultations, and real-time monitoring of patients performing CT tasks.

  • Patient Support

    TVCRP has access to a Patient Care Center that is the
    central hub for remote monitoring of the CT process.

  • Questions

    For more information about clinical trials, visit www.clinicaltrials.gov.

Truvision Clinical Research About (2)

Our Clinical Research Consortium Accelerates Trials

Our Clinical Research Consortium is a strategic alliance of clinical sites, contract research organizations (CROs), and industry sponsors—working together to transform how clinical trials are designed and executed. With a shared commitment to innovation, speed, and quality, the consortium streamlines operations across the trial lifecycle and ensures a more connected, efficient, and patient-centric research model.

A core pillar of our consortium is our Decentralized Clinical Trial (DCT) capability, which empowers sites and sponsors to reach broader, more diverse patient populations. Through remote monitoring, telemedicine, home health services, and digital data collection, we reduce participant burden, accelerate recruitment, and improve retention—all while maintaining data integrity and regulatory compliance.

Our Clinical Research Consortium is a strategic alliance of clinical sites, contract research organizations (CROs), and industry sponsors—working together to transform how clinical trials are designed and executed. With a shared commitment to innovation, speed, and quality, the consortium streamlines operations across the trial lifecycle and ensures a more connected, efficient, and patient-centric research model.

A core pillar of our consortium is our Decentralized Clinical Trial (DCT) capability, which empowers sites and sponsors to reach broader, more diverse patient populations. Through remote monitoring, telemedicine, home health services, and digital data collection, we reduce participant burden, accelerate recruitment, and improve retention—all while maintaining data integrity and regulatory compliance.

Clinical Research Consortium to Accelerate Trials

Truvision Clinical Research About (2)

Clinical Research Consortium to Accelerate Trials

Truvision Clinical Research About (2)

Our Clinical Research Consortium is a strategic alliance of clinical sites, contract research organizations (CROs), and industry sponsors—working together to transform how clinical trials are designed and executed. With a shared commitment to innovation, speed, and quality, the consortium streamlines operations across the trial lifecycle and ensures a more connected, efficient, and patient-centric research model.

A core pillar of our consortium is our Decentralized Clinical Trial (DCT) capability, which empowers sites and sponsors to reach broader, more diverse patient populations. Through remote monitoring, telemedicine, home health services, and digital data collection, we reduce participant burden, accelerate recruitment, and improve retention—all while maintaining data integrity and regulatory compliance.

Expertise That Drives Results

Collective Clinical Trials Experience Summary

Ophthalmology
  • Advanced Ocular Melanoma – Phase 2, multi-country
  • Ophthalmology (Device) Myopia Study – Phase 3 Single country
  • Ophthalmology (Device) Myopia Post-marketing – Phase 4
  • Single Country Ophthalmology Cataract Study – Phase 3 Multi-Country
Oncology
  • Cervical Intraepithelial Neoplasia – Phase 1/2a, multi-country
  • Metastatic Squamous Non-small cell Lung Cancer – Phase 3 Multi-country
  • Metastatic Non-squamous Non-Small Cell Lung Cancer – Phase 3, multi-country
  • Brain metastases from Non-small cell Lung Cancer – Phase 3 Multi-country
  • Peripheral T-cell Lymphoma – Phase 2 Single Country
  • Breast Cancer/Bone Pain – Phase 2b Multi-Country
  • B-Cell Lymphoma – Phase 3 multi country
  • Pancreatic Cancer – Phase 3 multi-country
Infectious Disease
  • SARs CoV2 (Covid-19) – Phase 2, single country
  • SARS CoV2 (COVID-19) – Observational Study, Single Country
  • Influenza Study – Phase 3, single country
Gastroenterology

Crohn’s Disease – Phase 3 Multi-Country

Cardiovascular
  • Angina – Phase 3, multi country
  • Atrial Fibrillation – Pilot Study, Single Center
  • Atherosclerosis Study – Phase 2 Multi-Center
  • Vertis CV-Diabetes Safety Study – Phase 3 Multi-Center
  • Chest Pain Study – Phase 3 Multi-Country
  • Hypertension Study – Phase 2 Multi-Country
Endocrinology
  • Type 1 Diabetes Study – Phase 2, Multi-Country
  • Type 2 Diabetes Study – Phase 2, Multi-Country
Urology/Oncology
  • Urinary Incontinence – Phase 3 Multi-Country
  • Overactive Bladder – Phase 3, multi-country
  • Prostate cancer – Phase 1, multi-country
  • Abarelix Prostate Cancer Study – Phase 3 Multi-Center
  • Vardenafil ED Study – Phase 3 Multi-Center
  • Lupron Prostate Cancer Study – Phase 3 Multi-Cente
  • Uprima ED Study – Phase 3 Multi-Center
  • Vasomax ED Study – Phase 3 Multi-Center
Nephrology

Chronic Kidney disease – Phase 3 multi-country

Psychiatry / Neurology
  • Anxiety Disorder – Phase 3 Single Country
  • Alzheimer’s Study – Phase 2 Multi-Center
  • Bipolar 1 Disorder – Phase 1&2, single-country
  • Schizophrenia with Ophthalmology Component – Phase 2 Single Country
  • Pain Management – Phase 3 Multi-Country
  • Major Depressive Disorder Study – Phase 2 Single Country
Hematology
  • Sickle Cell 1st in Human Study – Phase 1 Multi-Center
  • Sickle Cell Study – Phase 1 Multi-Center, Multi-Country
  • Sickle Cell Study – Phase 2/3 Multi-Country
Pulmonary / Rheumatology
  • COPD Study – Phase 2/3 Multi-Center
  • Gout Study – Phase 3 Multi-Country
Device Trials
  • Wound Healing Device Study – Phase 2 Multi-Center
  • Antibiotic Coated Penile Prosthesis – Phase 3 Multi-Center
  • Urinary Incontinence Device Study – Phase 3 Multi-Center
  • MIST BPH Study – Prospective Multi-Center Surgical study
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About Us

We are the leader in innovation & execution of comprehensive patient recruitment and
clinical trial management.

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