Our staff is GCP, IATA, and CCRP certified. We have a team of investigators, nurses, and other research support staff. Our average startup process takes less than 2 months. We have a robust recruitment process to assure enrollment of subjects in the appropriate clinical trials. We are committed to providing quality research.
Services
Full Clinical Trial Support
Investigator training
Coordination/Nursing Support
Quality Assurance
Infusion administration
In-house pharmacy
Resources
Dedicated exam room
Dedicated infusion room
Basic medical supplies
Vital signs, height and weight measurement
IV infusion pumps
On-site infusions
Refrigerated centrifuge
Ambient centrifuge
EKG machine
Emergency cart
AED
Oxygen tank and cannulas
Patient meal services
Lab processing area
Access to local lab
On-site investigational pharmacy
High speed internet
Secure limited access areas
Temperature control storage for drugs with limited access
Abundant free parking
Public transportation with convenient drop-off/pickup
Site Diversity Profile:
Diversity of study subject plays an important role. Inclusion of wide patient populations from various, races, ethnic groups, sex, genders, ages help provide evidence that the study product or device will be safe and effective and generalizable in the wider target patient pool if the drug or device is approved.
Site’s Race Profile
Site’s Ethnicity Profile
Site Start-up Timeline:
The startup process is an important part of the clinical trial and delays can have a huge impact on the cost of a study and ultimately the cost to develop a drug. At Prolato Research, we have an efficient start up process. From site selection to study activation, it takes average of 6 weeks. We use central IRB to expedite start-up process. In addition, contract, budget, and regulatory all can be done in parallel.