Quality. Integrity. Efficiency. Consistency.

We are committed to the highest integrity and execution through consistent communication with our clients and partners.

Services

The services provided by our company encompass every aspect of clinical research including:

Tailor fitting studies that work the best for the therapeutic area of the practice avoiding interference with current treatment plan of patients
Obtaining and negotiating contracts and budgets for clinical research studies
Managing clinical studies from study selection to close-out visit
Handling all regulatory affairs
Staffing and training where necessary
Developing standard operating procedures that will be strictly adhere to FDA regulations and NIH and GCP guidelines
Identifying potential study patients to meet enrollment and financial goals
Handling, retrieving, monitoring, and reporting data collected
Preparing for and/or facilitating external audits (FDA, IRB, Pharmaceutical)
Facilitating communication between the site and sponsor, CRO, and regulatory agencies.
Developing and maintaining standards in clinical research to assure human research protections and data integrity
Minimizing the amount of physician required time and involvement
Providing experienced, qualified and certified staff members for the conduction of clinical trials.

Professional development for Investigators participating in the clinical trials
Professional recognition in the community
Practices involved in clinical research remain at the cutting edge of its specific area of therapeutic interest
Clinical research in your therapeutic area offers alternative treatment to patients that competing practices will not have access to
The practice will generate auxiliary income with minimal impact on daily operations
Increase clinical trial awareness within the community
Physicians contribute to the development of new and innovative therapeutic treatments that are not yet available to the public