| Life Improvement Counseling Center Llc | |
|
418 Watt Street Jeffersonville IN 47130 | |
| (812) 288-8030 | |
| (812) 288-8032 |
| Full Name | Life Improvement Counseling Center Llc |
|---|---|
| Speciality | Counselor - Addiction (substance Use Disorder) |
| Location | 418 Watt Street, Jeffersonville, Indiana |
| Authorized Official Name and Position | Patricia Rose (CONTRACTING SPECIALIST) |
| Authorized Official Contact | 5024897122 |
| Accepts Medicare Insurance | This clinic does not participate in Medicare Program. |
| Mailing Address | Practice Location Address |
|---|---|
| Life Improvement Counseling Center Llc 418 Watt Street Jeffersonville IN 47130 Ph: (812) 288-8030 | Life Improvement Counseling Center Llc 418 Watt Street Jeffersonville IN 47130 Ph: (812) 288-8030 |
| NPI Number | 1427371426 |
|---|---|
| Provider Enumeration Date | 03/04/2010 |
| Last Update Date | 03/04/2010 |
| Identifier | Type | State | Issuer |
|---|---|---|---|
| 1427371426 | NPI | - | NPPES |
| Taxonomy | Type | License (State) | Status |
|---|---|---|---|
| 101YA0400X | Counselor - Addiction (substance Use Disorder) | (* (Not Available)) | Primary |
News Archive
A large observational study was presented at the Acute Cardiovascular Care 2019 a European Society of Cardiology (ESC) congress. It has found that heart attack patients survive longer if they are taken to heart centres early.
Routinely measuring fractional flow reserve using pressure wire assessment during coronary angiography for diagnosis of chest pain leads to significant changes in the management of one in four patients, according to results from a study reported at EuroPCR 2013.
High blood levels of C-reactive protein, a substance linked to inflammation, appear to be associated with an increased risk for age-related macular degeneration, according to a report in the October issue of Archives of Ophthalmology, one of the JAMA/Archives journals.
Three HMOs that administer managed care plans for Connecticut's Medicaid program must make public the rates they pay providers and other information, state Superior Court Judge George Levine ruled on Wednesday, the Hartford Courant reports.
SynCardia Systems, Inc., manufacturer of the SynCardia temporary CardioWest™ Total Artificial Heart, today announced it has received conditional approval from the U.S. Food and Drug Administration (FDA) to conduct an Investigational Device Exemption (IDE) clinical study of the Freedom™ driver system, the first-ever U.S. portable driver designed to power SynCardia's Total Artificial Heart.
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