INBRACE SUPPORT PROGRAM

Welcome to the Brand page for “INBRACE SUPPORT PROGRAM”, which is offered here for The mark consists of the stylized word inbrace in teal with a circle inside of the letter c shaded from teal to gold above the stylized words support program in gold.;the color(s) teal and gold is/are claimed as a feature of the mark.;promoting the interests of people who have parkinson's disease and their families and health care providers by means of public advocacy; promoting the interests of people who have friedreich's ataxia and their families and health care providers by means of public advocacy; promoting the interests of people who have congenital birth defects and their families and health care providers by means of public advocacy; promoting the interests of people who have rare pediatric epilepsies and their families and health care providers by means of public advocacy; promoting the interests of people who have scn8a developmental and epileptic encephalopathy and their families and health care providers by means of public advocacy; promoting the interests of people who have congenital adrenal hyperplasia and their families and health care providers by means of public advocacy; promoting the interests of people who have neurological diseases and their families and health care providers by means of public advocacy; promoting the interests of people who have central nervous system diseases and their families and health care providers by means of public advocacy; promoting the interests of people who have psychiatric diseases and their families and health care providers by means of public advocacy; promoting the interests of people who have movement diseases and their families and health care providers by means of public advocacy; promoting the interests of people who have endocrine diseases and their families and health care providers by means of public advocacy; promoting the interests of people who have hormonal diseases and their families and health care providers by means of public advocacy; promoting the interests of people who have genetic diseases and their families and health care providers by means of public advocacy;providing medical information regarding pharmaceutical products and services; pharmaceutical consultation, treatment support programs that coordinate insurance, drug delivery and prescription management between physicians, patients, and pharmacies; providing medical and health information in the field of parkinson's disease; providing medical and health information in the field of friedreich's ataxia; providing medical and health information in the field of congenital birth defects; providing medical and health information in the field of rare pediatric epilepsies; providing medical and health information in the field of scn8a developmental and epileptic encephalopathy; providing medical and health information in the field of congenital adrenal hyperplasia; providing medical and health information in the field of neurological diseases; providing medical and health information in the field of central nervous system diseases; providing medical and health information in the field of psychiatric diseases; providing medical and health information in the field of movement diseases; providing medical and health information in the field of endocrine diseases; providing medical and health information in the field of hormonal diseases; providing medical and health information in the field of genetic diseases;support program;creating an online community for people who have parkinson's disease and their families and health care providers for the purpose of engaging with and sharing information in the field of parkinson's disease; creating an online community for people who have friedreich's ataxia and their families and health care providers for the purpose of engaging with and sharing information in the field of friedreich's ataxia; creating an online community for people who have congenital birth defects and their families and health care providers for the purpose of engaging with and sharing information in the field of congenital birth defects; creating an online community for people who have rare pediatric epilepsies and their families and health care providers for the purpose of engaging with and sharing information in the field of rare pediatric epilepsies; creating an online community for people who have scn8a developmental and epileptic encephalopathy and their families and health care providers for the purpose of engaging with and sharing information in the field of scn8a developmental and epileptic encephalopathy; creating an online community for people who have congenital adrenal hyperplasia and their families and health care providers for the purpose of engaging with and sharing information in the field of congenital adrenal hyperplasia; creating an online community for people who have neurological diseases and their families and health care providers for the purpose of engaging with and sharing information in the field of neurological diseases; creating an online community for people who have central nervous system diseases and their families and health care providers for the purpose of engaging with and sharing information in the field of central nervous system diseases; creating an online community for people who have psychiatric diseases and their families and health care providers for the purpose of engaging with and sharing information in the field of psychiatric diseases; creating an online community for people who have movement diseases and their families and health care providers for the purpose of engaging with and sharing information in the field of movement diseases; creating an online community for people who have endocrine diseases and their families and health care providers for the purpose of engaging with and sharing information in the field of endocrine diseases; creating an online community for people who have hormonal diseases and their families and health care providers for the purpose of engaging with and sharing information in the field of hormonal diseases; creating an online community people who have genetic diseases and their families and health care providers for the purpose of engaging with and sharing information in the field of genetic diseases;.

Its status is currently believed to be active. Its class is unavailable. “INBRACE SUPPORT PROGRAM” is believed to be currently owned by “Neurocrine Biosciences, Inc.”