For sponsors and CROs
Community specialty sites with the patients your protocol needs.
For sponsors and CROs
Community specialty sites with the patients your protocol needs.
For sponsors and CROs
Community specialty sites with the patients your protocol needs.
Our founding network
Webuildresearchsitesinsideindependentspecialtypractices,whereyourtargetpatientsalreadyreceivecare.Ourfoundingnetworkisformingnow.Tellusaboutyourprotocol,andwewillmatchittotherightpractices.
Webuildresearchsitesinsideindependentspecialtypractices,whereyourtargetpatientsalreadyreceivecare.Ourfoundingnetworkisformingnow.Tellusaboutyourprotocol,andwewillmatchittotherightpractices.
Webuildresearchsitesinsideindependentspecialtypractices,whereyourtargetpatientsalreadyreceivecare.Ourfoundingnetworkisformingnow.Tellusaboutyourprotocol,andwewillmatchittotherightpractices.
Feasibility
How we answer your feasibility request
Clear answers, backed by real patient counts.
Share
Match
Start
Share your protocol
Send a synopsis or the full protocol. We sign a confidentiality agreement first and review it right away.
Share your protocol
Send a synopsis or the full protocol. We sign a confidentiality agreement first and review it right away.
We match practices and count patients
We find practices and investigators that fit your study. Then we pull de-identified patient counts from each practice's own records.
We match practices and count patients
We find practices and investigators that fit your study. Then we pull de-identified patient counts from each practice's own records.
Site startup
One team handles regulatory documents, the budget, and the contract. A trained coordinator is in place before the site is activated.
Site startup
One team handles regulatory documents, the budget, and the contract. A trained coordinator is in place before the site is activated.
Research standards
Built on the standards sponsors trust
Every Whizz site follows the rules that govern industry research.
ICH Good Clinical Practice
How studies are run, documented, and monitored, and how participants are protected.
ICH Good Clinical Practice
How studies are run, documented, and monitored, and how participants are protected.
Informed consent
21 CFR Part 50. What each participant must understand and agree to before joining a study.
Informed consent
21 CFR Part 50. What each participant must understand and agree to before joining a study.
Informed consent
21 CFR Part 50. What each participant must understand and agree to before joining a study.
IRB review
21 CFR Part 56. Independent ethics oversight of every study protocol.
IRB review
21 CFR Part 56. Independent ethics oversight of every study protocol.
IRB review
21 CFR Part 56. Independent ethics oversight of every study protocol.
HIPAA
Patient privacy, with a business associate agreement at every site.
HIPAA
Patient privacy, with a business associate agreement at every site.
HIPAA
Patient privacy, with a business associate agreement at every site.
Electronic records
21 CFR Part 11. Rules for electronic records and electronic signatures.
Electronic records
21 CFR Part 11. Rules for electronic records and electronic signatures.
FDA drug and device rules
21 CFR Parts 312 and 812. Investigator duties for investigational drugs and devices.
FDA drug and device rules
21 CFR Parts 312 and 812. Investigator duties for investigational drugs and devices.
FDA drug and device rules
21 CFR Parts 312 and 812. Investigator duties for investigational drugs and devices.
What you get
Every feasibility response includes
No inflated numbers. If a site is not a fit, we tell you.
Real patient counts
De-identified counts of patients with your target condition, pulled from the practice's own records.
Investigator background
The PI's specialty, board certification, procedure experience, and GCP training.
Site capabilities
Rooms, equipment, imaging, lab processing, and storage, checked against your protocol.
Site capabilities
Rooms, equipment, imaging, lab processing, and storage, checked against your protocol.
A startup plan
The named coordinator, the regulatory timeline, and our recruitment plan for your study.
Sponsor FAQ
Questions from sponsors and CROs
Where are your sites?
Our founding network is forming now. Tell us your study's target regions, and we will tell you honestly whether we can support them.
Can a physician new to research lead a study?
What study types do you support?
How do you recruit patients?
Who is our point of contact?
How do we start?
Where are your sites?
Our founding network is forming now. Tell us your study's target regions, and we will tell you honestly whether we can support them.
Can a physician new to research lead a study?
What study types do you support?
How do you recruit patients?
Who is our point of contact?
How do we start?
Tell us about your study
Send a synopsis for a free feasibility review. We reply within one business day.
Plain-English research guides, sent when we publish.
We never share your email.
For practices
For sponsors
© 2026 Whizz Health LLC. All rights reserved.
Whizz Health does not provide medical care. Studies at partner practices are overseen by licensed physicians.
Plain-English research guides, sent when we publish.
We never share your email.
For practices
For sponsors
© 2026 Whizz Health LLC. All rights reserved.
Whizz Health does not provide medical care. Studies at partner practices are overseen by licensed physicians.
Plain-English research guides, sent when we publish.
We never share your email.
For practices
For sponsors
© 2026 Whizz Health LLC. All rights reserved.
Whizz Health does not provide medical care. Studies at partner practices are overseen by licensed physicians.