Our Services

Research Site Set-up

  • 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.

Study Acquistion

  • Using strategic partnerships with biotechs, 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.