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.

 
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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.