Our Services
Phase I Services
We offer comprehensive Phase I clinical trial services dedicated to drug and devise research. Our integrated procedure room allows us to perform a variety of surgical type studies. The surgical studies are often combined with Phase I study designs in order to obtain early Phase II results. Our research professionals have the skills, expertise and assets to provide rapidly7 enrolling early phase development programs. With capabilities of housing up to 70 subjects for in-patient protocols along with our state-of-the art equipment, we can accommodate most Phase I trials. Our services can be bundled or tailored to meet our client’s needs.
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Protocol/CRF/Source Document Development
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Participant recruitment
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Study execution and conduct
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Quality assurance
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QT & QTc studies
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Continuous telemetry
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Single or Multiple dose range studies (SAD/MAD)
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Maximum Tolerated Dose (MTD) studies
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Pharmacokinetic and Pharmacodynamic studies
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Abuse liability
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ADME Studies
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Sleep Lab Studies
Phase I-IV
Services
Patients &
Strategic Alliances
Phase II -IV Services
Aspen Clinical Research provides comprehensive services supporting Phase II-IV Clinical Pharmacology and device activities. We use our internal expertise across all therapeutic areas as well as our affiliations with other clinical sites, hospitals and CROs to support your development needs.
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Study feasibility and protocol development
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Multi Center Recruitment
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Inpatient/Outpatient Trials
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Proof of Concept Studies
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Studies to Support Label Claims
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Safety and Efficacy Studies
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Hospital and University Collaborations for Patient Population Recruitment
Phase I-IV Protocol Design
Protocol design can be a complicated and argues process if you don’t employ the right team of professionals. We have over 14 years of experience in protocol writing, study setup, execution and study conduct. We also have an in house skilled medical writer to assist with preparation and submission. We believe that the more sound a protocol is designed the more scrutiny it will stand on the back end. The final product is a clean data set due to the upfront leg work in the protocol design.
Bioequivalency/Bioavailability Studies
We have a team of professionals highly experienced in setting up, executing and conducting Bioequivalency and Bioavailability drug testing. Our team has performed several bio equivalence clinical trials for a variety of industry-leading pharmaceutical companies. Our facility is located within 5 miles of two major universities in Utah County. Combined with Aspen’s experienced team and strategic location we have the ability to set up, enroll, execute, and conduct these types of studies. Our services include the following:
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Protocol development
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Participant recruitment
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Study execution and conduct
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Quality assurance
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QT & QTc studies
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Continuous telemetry
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Pharmacokinetic and Pharmacodynamic studies
Patient Recruitment
Critical timelines are our specialty. Rapid response by your Central IRB combined with our network of community, clinic database of 125,000 patients and social media, provides our recruitment department the ability to meet or exceed our projected enrollment goals timely and effectively.
Strategic Alliances
We have strategic alliances with community health care clinics, private practice providers, and other healthcare networks to allow access to a large variety of potential subjects with a multitude of clinical indications and conditions. We also have coordinated and provided subject transportation and access to special populations bases, i.e. hospice patients, diabetic patients, patients that recently received various surgery/procedures, patients whom have or do reside in the LTC facilities, etc.
Our diversified approach works at our competitive advantage to provide the community with leading Phase I-IV research to help prevent, diagnose and treat diseases. We are proud to have successfully helped our clinical partners expedite many pharmaceutical product and devices through the development process safely and efficiently.
Utah Chapter
Utah Chapter