Step One Tour our Facility
We will schedule a meeting with you and our team to guide you through our facility. You will see first hand what equipment and facilities are available for your study. You get to meet the staff who will be supporting your clinical study, and most importantly, you will see how the HPCRL can enhance your research and give the best possible clinical experience for your subjects.
Step Two Feasibility
After your tour, and you are excited to get the ball rolling, we will sit down with you to work out the nuts and bolts. Like we said, we know how to get you from your initial hypothesis to completing data analysis. We will discuss budgeting, testing, and data collection requirements. We will help you design a tailor-made plan to complete your study on time and within your budget.
Step Three Planning
Taking the time to develop a thorough plan is a certain recipe for success. Because we do this every day, we know what works and how to help you develop an airtight plan. This may include training, scheduling, IRB development, or participant recruitment. Data collection and data storage is also an important part of the plan. We help you keep it all organized and centrally located with our data capture, and data management services. Finally, we set up an invoicing plan to help you easily track your expenses and streamline your payments.
Step Four Training
We are proud of the culture of safety we have fostered through extensive training in a supportive environment for all personnel involved in HPCRL research.
Our staff is also trained in the most current FDA and NIH requirements for conducting clinical trials. We will develop a training plan to suit the needs of your study.