Our team’s objective is to provide you with experienced, qualified clinical research sites for a successful and timely completion of a study.

We create well-established working relationships at each site and implement our Strategic Clinical Study Management Plan to ensure excellence and precision throughout the life of the study.

• We engage in routine communication with all of our sites.
• We provide study update reports to our sites.
• We review enrollment goals and discuss recruitment strategies.
• We schedule regular meetings with both the CRC and Physician.

Our Sponsor services include:

Site Qualification Development

• Pre-qualify sites to ensure study is a good fit and enrollment goals can be met
• Site information packets provided to CRA
• Site visit preparation (e.g. protocol and equipment review)
• Site visit date and time coordination

Document Processing

• Regulatory document completion within 7-10 business days
• Centralized contract and budget negotiations within 7-10 business days
• Central IRB submission

Site Management

• Thorough up-to-date CV, licensure and training certification review
• Standard Operating Procedures (SOP) binders
• Patient recruitment marketing services
• Identify process improvement areas and implementation

Sponsors/CROs relationships

Abbott			Merck
Abbvie			Novartis
Alcon			Novo Nordisk
Amgen			Parexel
Bausch and Lomb			Pfizer
Boehringer Ingelheim			Pharma-Olam
Chiltern			Purdue
Eli Lilly			Quintiles
Eyegate			Salix
Forest			Smith and Nephew
Furiex			SGS
Genentech			Symbio
GSK			Synergy
Inotek			Takeda
Inventiv			UBC
Medpace			Zimmer