Pharmaceutical Sponsors

At Clinical Endpoints, we specialize in providing personalized, concierge-level services to our patients through world-class health care professionals. We understand the importance of personalized patient services, as well as the hope that promising clinical trial treatments may bring to our physician partners, their patients and their families.

Our concierge-level service begins with our expert staff. Our team is led by renowned Board Certified physicians that partner with us to provide first-class patient services. The clinical staff that support our physician team are highly trained and experienced clinical care and research coordinators that are fully certified in all regulations required for the specialized care required by clinical trials.

Our staff performs all regulatory submissions, patient recruitment, marketing and business development. We recognize that strong recruitment contributes to the success of a clinical trial. That is why at Clinical Endpoints we partner with physicians who are motivated to provide research as another treatment option to their patients. This referral stream leads to the site exceeding enrollment goals and reducing screen failures. We are typically the leading enroller of patients globally for the trials we choose to offer to our patients.

At Clinical Endpoints our goal is to provide supportive service and education to our patients and their families as well as demonstrate clinical excellence through our dedication to clinical trials.

• Validated 24-hour temperature monitoring system with alarm
• Backup Battery System on all refrigeration equipment
• Calibrated Vitals Machine/Scale
• 12 Lead Electrocardiogram
• Calibrated Ambient Centrifuge
• Calibrated Refrigerated Centrifuge
• Designated, secure and temperature monitored Drug Storage
• Secured maintenance of clinical trial documents/records both on and off site.
• Working lab and designated blood draw room
• -20° Freezer
• -80° Freezer
• Dedicated IV Infusion room
• Dedicated Rater room for study assessments
• Spacious and immaculate exam suites

Access to accredited full-service radiology unit through our affiliate company (walking distance from our facility)

Access to accredited local laboratory facility to perform Lumbar Puncture

• Available Central Institutional Review Board (IRB)
• Regulatory Packets are completed within 1 week of receipt
• Contracts and Budgets completed within 2 weeks of receipt
• GCP Trained Research Professionals
• Comprehensive and time-proven Standard Operating Procedures (SOPs)
• Protocol development expertise on-staff
• Source documentation development expertise on-staff
• IATA/hazardous shipping certification
• 24-hour emergency contact
• Dedicated monitoring area
• Onsite & offsite storage facility
• All equipment is inspected and calibrated pursuant to strict site procedures

At Clinical Endpoints we have the integrated capability to perform Phase I-IV clinical trials.

Not limited to the following indications: