We would like to provide outstanding training and support investigative sites in order to ensure subject safety and data quality during a conduct of clinical trials.
We would like to apply our experience in the field of science and research with the aim of supporting clinical research sites helping them stay in compliance with international standards of Good Clinical Practice, local regulations and FDA regulations.
For Investigative Sites
Do you have Clinical Studies and tools you need?
We work with Sponsors to obtain Clinical Trials according to site staff experience and site capabilities
We provide consulting services and tools to selected sites to help them to obtain studies and be in compliance with protocol requirement, FDA regulations and Good Clinical Practices.
Would you like to be among the best Investigative Site?
We are selecting a limited numbers of Sites to work with them providing studies according to site staff experience and site capabilities, consulting services, training and audits.
Are you looking for outstanding sites?
We understand that sponsors need excellent investigative sites to conduct their studies.
We have a partnership with a network of sites/Investigators in South Florida region. They can conduct studies in several therapeutic areas. We supervise all studies conducted for our investigators during the study conduction (from site selection to close out) providing training, consulting services and auditing our sites to keep them in compliance with protocol, regulations and GCP.
When you select one of our investigators to conduct a clinical trial; you know that we are overseeing your studies to provide our sites Quality Assurance and Quality control.
Phone: +1 305 610-3464
Fax: 1 866-2784140