Research Solutions Unique to your study
Let us provide you with high-quality healthcare and research
About Us
Generate excitement
Generate excitement
Generate excitement
Evidence-based scientific research methods
Grab interest
Generate excitement
Generate excitement
every problem has a solution
Feature something
Generate excitement
Feature something
Innovative solutions unique to your research
Who We Are
Clinical Trial Specialists, You Can Trust
Feel confident in the field of your research specialty. We specialize in clinical research study start-ups and provide support staff and assistance with regulatory submission requirements for Institutional Review Board submissions. If you are a research scientist/Principal Investigator new to clinical research, we will walk you through the process and train your clinical team. Our expertise includes support and consultation for all private- industry or NIH-sponsored Investigative Medicinal Products and Investigative Medical Devices to an array of clinical studies that do not include human subjects. Whether you need daily or weekly assistance due to regulatory issues, study deviations, staff training, or need for licensed temporary staff.
Experienced and Supportive
We understand that not one study plan fits all. Our daily services include staff support, regulatory documentation assistance, Electronic Data Collection, and Data entry. We provide IRB documentation preparation, statement of Investigator form FDA 1572 completion assistance, and supervision of study-related activities. We will take the time to get to know you and your research team and develop an individualized study plan for recruitment, enrollment, and retention strategies that fits your clinical study's specific needs.
We provide experienced licensed clinical staff at a subsidized cost for the timely launch of your research study. Our list of services includes the onsite organization of logistics, detailed explanation of the launch process of a new clinical study, legal documents and submissions needed for IRB submissions, Seamless and speedy launch of IRB-approved clinical studies, availability of licensed and experienced healthcare staff for initial study launch support and training of permanent study team. Minimizing study deviations by assisting the study team, Ensuring that clinical studies are completed and endpoint data collected, Helping the study team in training for electronic data collection
Testimonials
Dr. Padmashri
“If you are looking for some awesome, knowledgeable people, these are the people I highly recommend. Their friendliness and result-driven approach is what I love about them."
“I didn’t know what to do about my grants . I found that this team was just who I was looking for. They are friendly, professional, and they really care.”
anonymous
"If you are looking for some compassionate, caring people, this is the team I highly recommend. Their friendliness and professionalism are what I love about them."
Reviews
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