Seeking greater returns for your clinic?
HealFlow LLC facilitates clinical research as part of your medical practice, even if you’re new to research.
Your role as a Principal Investigator (PI) can benefit patients, your practice, your career, and the practice of medicine. But most notably, it can improve your bottom line. Many PI’s earn an additional 50% of their medical practice profit by adding clinical research.
what about the barriers to research?
Perhaps you dismissed clinical research because you lack the time, energy, staff, infrastructure, access, and/or know-how to get started.
We understand these legitimate barriers and we can help...
• Bringing relevant, new research projects into your practice
• Doing most of the work for you
• Handling most of the regulatory effort
• Taking accounting, billing, collecting, off your hands, and
• Training you to oversee research as a Principal Investigator
Imagine your practice with more income, patients, security, and value…
Clinical research isn’t easy, but it offers numerous rewards:
Significant new, income – Become less dependent on existing cash-flow sources - earn substantial additional profit without extra Medicare, insurance, coding, and billing.
More valuable practice - Greater income increases the value of your practice, when you choose to sell.
New patients – Our local marketing will improve your practice’s visibility.
Publishing and speaking – Clinical research is a gateway to paid speaking as a Key Opinion Leader
New patient options – Give your patients the opportunity to get involved in research.
Fulfillment – Know that many people may benefit from your research, combatting disease and advancing medicine.
Professional growth – Expand your capabilities as a top-notch physician; Provide new training and growth opportunities for your staff.
What does HealFlow do for you?
(Hint: Heavy lifting)
We Get Clinical Trials Done.
We secure appropriate research projects, provide an experienced study coordinator to manage the entire process from start to finish, train you (and your team where applicable), and minimize distraction to your practice. You enjoy a stake in each project.
Specifically, we:
· Bring research opportunities relevant to your patient population
· Assist with Feasibility Surveys and Site Selection Visits for new studies
· Negotiate budgets and contracts with Sponsors to maximize your income
· Manage regulatory requirements including all necessary documentation
· Train you (and your staff as needed)
· Oversee study management
· Complete source documents
· Define the SOPs and update them as they evolve
· Work with the clinical study monitor both remotely and onsite
· Communicate with the sponsor and IRB
· Plan and schedule research
· Consent participants
· Collect and transcribe data
· Recruit additional participants outside the practice
· Bill and collect
…and other clinical trial related activities
