FTD Disorders Registry Revenue
Research Services • 
King of Prussia, Pennsylvania, United States • 1-10 Employees
FTD Disorders Registry revenue & valuation
| Annual revenue | $427,775 |
| Revenue per employee | $86,000 |
| Estimated valuation?This valuation is estimated based on industry average for the Research Services industry and current estimated revenues | $1,400,000 |
| Total funding | No funding |
Key Contact at FTD Disorders Registry
Carrie Milliard
Director, FTD Disorders Registry
Company overview
| Headquarters | King of Prussia, Pennsylvania, United States |
| Phone number | +120162025 |
| Website | |
| NAICS | 5417 |
| Keywords | Community Engagement, Neurological Disorders, Family Members, Collaborative Partnerships, Ftd Patient Registry (For Diagnosed Persons, Frontotemporal Degeneration (Ftd), International Contact Registry, North American Research Registry, Behavioral Variant Ftd (Bvftd), Caregivers & Friends), Clinical Study Recruitment, Corticobasal Degeneration (Cbd), De-Identified Data (Guid Protects Privacy), Online Data Collection Portal, Patient-Centric Research, Primary Progressive Aphasia (Ppa), Progressive Supranuclear Palsy (Psp), Rare Dementia Diseases, Registrant Surveys |
| Founded | 2015 |
| Employees | 1-10 |
| Socials |
FTD Disorders Registry Email Formats
FTD Disorders Registry uses 3 email formats. The most common is {first initial} (e.g., j@ftdregistry.org), used 50% of the time.
| Format | Example | Percentage |
|---|---|---|
{first initial} | j@ftdregistry.org | 50% |
{first initial}{last name} | jdoe@ftdregistry.org | 25% |
{first name} | john@ftdregistry.org | 25% |
About FTD Disorders Registry
The FTD Disorders Registry is an online database to collect information from those affected by all types of frontotemporal degeneration (FTD): behavioral variant FTD (bvFTD), any one of the primary progressive aphasias (PPA), progressive supranuclear palsy (PSP), corticobasal degeneration (CBD), or FTD with motor neuron disease (also called FTD-ALS). The FTD Disorders Registry (FTDDR) is designed to bring together the frontotemporal degeneration community, this means persons diagnosed, their family members, caregivers, and friends as well as clinicians, scientists, and industry. Our goal is to work together to bring treatments and cures to this spectrum of disorders. The FTDDR is both a Contact Registry and a Research Registry. As a Contact Registry persons affected by FTD, their caregivers, family members, and friends can join and receive emails about FTD including important research updates and study opportunities. Contact Registry enrollment is open to the US and international community. As a Research Registry, persons diagnosed, their caregivers, family members, and friends can provide their unique perspective to help us learn more about FTD. Research Registry enrollment requires an individual to be at least 18 years of age and a resident of the US or Canada (19 years in those states or provinces where the age of majority is 19; Alberta, Saskatchewan, Newfoundland and Labrador currently excluded).
Employees by Management Level
Total employees: 1-10
Seniority
Employees
Funding Data
FTD Disorders Registry has never raised funding before.
FTD Disorders Registry Tech Stack
Discover the technologies and tools that power FTD Disorders Registry's digital infrastructure, from frameworks to analytics platforms.
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Frequently asked questions
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