Boost Your Practice by Conducting Clinical Trials
Increase Practice Visibility
Many of the patients you already see in your private practice will qualify for a clinical trial. Additionally, patients from outside your practice who are seeking specific study will be led to your practice, expanding your reach and impact.
Enhance Patient Care
Offering clinical trials to your patients allows your practice to provide novel therapies before becoming widely available.
Patients that participate in a clinical trial report a better understanding of their condition.
Increase Revenue
Private practices with a stable patient population can significantly increase revenue by participating in a clinical trial. Each study patient visit generates a new income for the practice.
Our Services
Many private practices miss out on the benefits of clinical research such as enhanced patient care and increased revenue because they assume clinical trials are too complex and time consuming. With our help these practices can obtain the benefits of clinical research while maintaining their current workload.
Using collaboration, industry expertise and developed Standard Operating Procedures (SOPs) Archway provides research site infrastructure creation. We ensure the site is in full compliance with the IRB, FDA, and GCP regulations.
Research Site Set-up
Study Acquistion
Using strategic partnerships with biotech companies Clinical Research Organizations (CROs) and pharmaceutical companies we are able to obtain a large variety of clinical studies
We match practices with high value clinical studies that fit their patient population. Archway Clinical ensures practices have a diverse study portfolio to negate industry ups and downs.
Research Site Support
After the creation of a research site, we continue to provide support to optimize success. Support includes:
Regulatory oversight, financial reporting and profitability tracking, technical system support, continual review and revision of site Standard Operating Procedures (SOPs), creation of study specific source documents and site staff recruitment.