Enhance
your practice
through clinical
research.

Injury Care and Family Care Research are currently partnering with physicians in the Boise area.

Our mission is to conduct trials that seek to progress the quality of life and health of all by the development of new medications and devices that aid in advancing modern healthcare management and increasing our knowledge of disease. We are committed to providing our clinical research participants with the highest quality care and our study sponsors with optimum clinical data.

Benefits to Your Practice

• Increased income through Principal Investigator fees and additional patient visits

• Opportunity to offer alternative therapies to patients

• Positions your practice at the forefront of new patient therapies

• Family Care Research assumes the up-front risk and minimizes your time requirements

• The flexibility to see patients at your facility or ours

Benefits to Your Practice

• Increased income through Principal Investigator fees and additional patient visits
• Opportunity to offer alternative therapies to patients
• Positions your practice at the forefront of new patient therapies
• Family Care Research assumes the up-front risk and minimizes your time requirements
• The flexibility to see patients at your facility or ours

Coordination of Clinical Trials

Family Care Research manages all aspects of the clinical trial, including all study procedures – subject consent, medical histories, performing ECGs, vitals, lab draws, etc. We also resolve queries, monitor and audit visits as required by the FDA, and oversee drug accountability. This includes shipping of hazardous materials. Family Care Research uses CRIO’s eSource software for all study documentation.

Regulatory Documentation

Family Care Research administers all regulatory procedures including submission to the Institutional Review Board (IRB), protocol training implementation and documentation, ongoing regulatory maintenance and closeout of study documentation at the end of each protocol. We utilize Complion’s state-of-the-art eRegulatory Documentation software.

Contracts and Budget

All contracts (Confidentiality Agreements, Clinical Trial Agreements, etc.) and budgets are negotiated by a Certified Clinical Research Contracts Professional (MAGI). Additionally, a contract attorney is maintained on retainer for any necessary consultations regarding contract language or implementation.

Accounting

We utilize CRIO’s Clinical Trial Management Software program to manage all study payments both from study sponsors as well as to vendors, physicians and subjects for subject visit stipends.