Family Medicine Of Indiana | |
9640 N Augusta Dr Suite 413 Carmel IN 46032-9600 | |
(317) 334-1900 | |
(317) 334-1901 |
Full Name | Family Medicine Of Indiana |
---|---|
Speciality | Family Medicine |
Location | 9640 N Augusta Dr, Carmel, Indiana |
Authorized Official Name and Position | Millicent D. Moye (CEO) |
Authorized Official Contact | 3173341900 |
Accepts Medicare Insurance | This clinic does not participate in Medicare Program. |
Mailing Address | Practice Location Address |
---|---|
Family Medicine Of Indiana 9640 N Augusta Dr Suite 413 Carmel IN 46032-9600 Ph: (317) 334-1900 | Family Medicine Of Indiana 9640 N Augusta Dr Suite 413 Carmel IN 46032-9600 Ph: (317) 334-1900 |
NPI Number | 1336368810 |
---|---|
Provider Enumeration Date | 04/24/2007 |
Last Update Date | 06/06/2008 |
Identifier | Type | State | Issuer |
---|---|---|---|
1336368810 | NPI | - | NPPES |
000000521092 | Other | IN | ANTHEM |
100143130 | Medicaid | IN |
Taxonomy | Type | License (State) | Status |
---|---|---|---|
207Q00000X | Family Medicine | 01059510A (Indiana) | Primary |
News Archive
Patients with high levels of proteinuria (protein in urine) in addition to another marker of reduced kidney function had an associated increased risk of all-cause death, heart attack or progression to kidney failure, according to a study in the February 3 issue of JAMA.
Several groups across the healthcare sector will rollout two new "Personal Health Record Quick Reference Guides" in an effort to educate consumers and clinicians about how PHRs can be useful tools for making more informed healthcare decisions and enhancing care coordination.
Clerity Healthcare, a leading provider of end-to-end IT solutions, today announced that it has been selected by GE Healthcare as the exclusive systems integration technical solutions provider for GE Centricity Practice Solution and Centricity Electronic Medical Records (EMR) customers.
Queensland University of Technology (QUT) world-first research has found a link between increases in temperature and the incidence of stillbirth and shorter pregnancies.
QLT Inc. today announced results from Phase II clinical trials and a device study for the punctal plug delivery system (PPDS). These studies are part of a development program that is being conducted by QLT's wholly-owned subsidiary, QLT Plug Delivery, Inc. QLT also announced its plans to expand the program to evaluate a second drug for a new target indication.
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