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NORD ASKI REGIONAL ECONOMIC DEVELO

HEARST-Canada

Company Name:
Corporate Name:
NORD ASKI REGIONAL ECONOMIC DEVELO
Company Title:  
Company Description:  
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Company Address: 1500 Front St,HEARST,ON,Canada 
ZIP Code:
Postal Code:
P0L 
Telephone Number: 7053627355 
Fax Number:  
Website:
 
Email:
 
USA SIC Code(Standard Industrial Classification Code):
78200 
USA SIC Description:
ECONOMIC DEVELOPMENT AGENCIES 
Number of Employees:
 
Sales Amount:
$2.5 to 5 million 
Credit History:
Credit Report:
Excellent 
Contact Person:
 
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Company News:
  • Financial Assistance For Patients With Rare Diseases | NORD
    NORD’s Rare Caregiver Respite program was an absolute lifeline for our family this past year With the respite program, I was able to select a family friend who I trusted, who was already adequately trained to handle my daughter’s needs, and I could have her provide respite whenever I needed it The reimbursement process was easy, and payment was received promptly
  • Centers of Excellence - National Organization for Rare Disorders
    NORD is committed to breaking down silos and building bridges so that people living with a rare disease can achieve their best health and well-being Our belief is that the NORD Rare Disease Centers of Excellence program is the next big stride forward for rare disease patients and care, to improve health equity and create critical new connections to resources and specialists across our nation
  • List of Rare Diseases | A-Z Database | NORD
    What Is the NORD ® Rare Disease Database? The NORD Rare Disease Database is an inclusive and comprehensive list of rare diseases based on information from established rare disease ontologies and it is an ongoing project made possible by a close collaboration with MONDO, Orphanet, and Online Mendelian Inheritance in Man (OMIM) The NORD Rare Disease Database includes: NORD Rare Disease Reports
  • About Us - National Organization for Rare Disorders
    NORD was the first national nonprofit to represent all individuals and families affected by rare disease Today we’re the only organization working at the intersection of care, research, policy, and community for all rare diseases
  • Contact Us - National Organization for Rare Disorders
    Contact Us NORD is leading the fight to improve the lives of patients with rare diseases For more information or to learn more, use the contact details below or sign up for email communications here So that we can best assist you, please use the form below if you are seeking additional information from our team Please submit your inquiry only once to ensure a timely response
  • Rare Disease Research Grant Program | NORD
    Request for Proposals NORD’s Rare Disease Research Grants Program provides seed-money grants to qualified investigators for scientific and or clinical research The hope is that these studies ultimately will lead to new diagnostics, treatments, and or cures for rare diseases NORD’s program provides grants for the study of diseases for which there are few other sources of funding Grants
  • Rare Diseases Support, Resources Help | NORD
    Can NORD help find a medical expert for my rare disease? Many patient organizations provide lists of medical experts Search NORD’s Organizational Database to find disease-specific patient advocacy organizations NORD Rare Disease Centers of Excellence are diagnosing and treating thousands of rare disease patients
  • Patient Assistance Programs - National Organization for Rare Disorders
    Since 1987, NORD has provided assistance programs to help patients obtain life-saving or life-sustaining medication they could not otherwise afford These programs provide medication, financial assistance with insurance premiums and co-pays, diagnostic testing assistance, and travel assistance for clinical trials or consultation with disease specialists
  • About NORD Membership Network | NORD
    While some of these resources are free, the full range is only available to NORD network members We offer 2 levels of membership: Platinum Level represents the highest level of integrity and transparency for patient advocacy organizations involved in medical research, drug development, medical education, and registries




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