End-to-End Clinical Trial Services in a Cutting-Edge Facility
Our Kissimmee facility is designed to provide a seamless and comprehensive clinical trial experience, from initial planning and patient recruitment to regulatory compliance, data integrity, and post-study care. With an experienced team and a full suite of specialized services, we are equipped to support every phase of your clinical trial with precision and efficiency.
We prioritize both patient safety and data accuracy through rigorous quality assurance protocols, secure data management systems, and robust patient engagement strategies.
From dedicated pre-screening and enrollment spaces to specialized rooms for data capture and patient monitoring, each aspect of our facility is designed to support high-quality research and smooth trial execution. We understand the importance of a controlled, compliant environment and have invested in the best resources and technologies to support reliable outcomes.
Our team’s commitment to excellence and patient-centered care ensures that each study conducted here meets the highest standards of integrity and effectiveness, allowing you to focus on advancing impactful research.
Premier Medical Research Space
Modern facility designed for seamless clinical trial operations and optimal patient care
Located in the heart of Kissimmee, our facility offers convenient access for participants, sponsors, and CROs. Equipped with advanced technology and a comfortable environment, our space is designed to meet the highest standards of clinical research.
Features of our facility include:
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Centralized Location: Easy access for patients and partners from across Kissimmee.
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Advanced Equipment: Equipped with modern tools for data collection, lab testing, and patient monitoring.
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Comfortable Patient Areas: Our welcoming and comfortable spaces enhance the patient experience, ensuring they feel supported throughout each visit.
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On-Site Pharmacy and Lab Services: Offering in-house testing and secure medication storage for seamless study management.
Our facility is dedicated to upholding safety, privacy, and regulatory standards, providing a reliable environment for comprehensive clinical research services.
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Patient Recruitment & Retention
We specialize in patient recruitment strategies tailored to meet the specific needs of your study. Our team conducts thorough pre-screening, screening, and enrollment processes to ensure the right participants join the study, supporting high retention rates through engaging, patient-centered programs.
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Study Coordination & Management
From scheduling visits to coordinating procedures, we handle every detail to ensure your study runs smoothly. Our meticulous record-keeping practices support regulatory compliance, and our strong communication with sponsors and CROs keeps every stakeholder informed and involved.
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Regulatory Compliance & Documentation
Our team handles every aspect of regulatory compliance, from preparing submissions for Institutional Review Boards (IRBs) to maintaining essential regulatory documentation. We strictly adhere to Good Clinical Practice (GCP) and FDA guidelines to uphold the integrity of each study.
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Data Collection & Quality Assurance
We ensure the accuracy of data through meticulous collection and quality assurance protocols. Using Electronic Data Capture (EDC) systems, we securely store and transmit data, maintaining compliance and data integrity throughout the study process.
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Patient Care & Monitoring
Our facility is designed to prioritize patient safety and comfort throughout the trial. Our team conducts regular health assessments and safety monitoring to ensure participants’ well-being, with robust adverse event reporting processes and aftercare support.
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Pharmacy & lab services
For studies that require it, our facility offers on-site lab testing and secure drug storage. Our pharmacy services adhere to strict compliance protocols to ensure accurate drug handling, storage, and dispensing.
What We Offer
Q: What makes Cliniquest a trusted partner in clinical research?
A: Cliniquest offers unmatched expertise and top-tier facilities that drive clinical studies to success. We specialize in all trial phases (Phases 2-4) across diverse specialties, providing seamless progress from early development to late-stage trials.
Q: Does Cliniquest cover various therapeutic specialties?
A: Yes, we support a wide range of therapeutic areas, allowing sponsors access to diverse patient populations and tailored study requirements—all within a single facility.
Q: How does Cliniquest manage studies from start to finish?
A: We provide end-to-end study management, handling everything from feasibility assessments and patient recruitment to protocol adherence and data integrity. Quality, consistency, and efficiency are our top priorities in every trial phase.
Q: How quickly can Cliniquest start a new study?
A: Our streamlined processes allow us to reach site readiness within as little as four weeks after contract finalization, enabling studies to launch without delay.
Q: How does Cliniquest handle data entry for studies?
A: We prioritize real-time data entry, with data logged the same day it's collected or by the next business day. This minimizes delays and ensures data accuracy, supporting timely access to critical information for ongoing analysis.
Interested in exploring partnership opportunities? We’d love to discuss how Cliniquest can contribute to the success of your clinical trials.
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