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.
- Protocol/CRF/Source Document Development
- Participant recruitment
- Study execution and conduct
- Quality assurance
- QT & QTc studies
- Continuous telemetry
- Single or Multiple dose range studies (SAD/MAD)
- Maximum Tolerated Dose (MTD) studies
- Pharmacokinetic and Pharmacodynamic studies
- Abuse liability
- ADME Studies
- Sleep Lab Studies
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.
- Study feasibility and protocol development
- Multi Center Recruitment
- Inpatient/Outpatient Trials
- Proof of Concept Studies
- Studies to Support Label Claims
- Safety and Efficacy Studies
- 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.
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