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Hemophilia Society (lucknow) Ngo Information
Registration Details
Registered With
Registrar of Societies
Type of NGO
Registered Societies (Non-Government)
Registration No
1271
Copy of Registration Certificate
Available
Copy of Pan Card
Available
Act name
Societies Registration Act, 1860
City of Registration
LUCKNOW
State of Registration
UTTAR PRADESH
Date of Registration
14-08-1997
Foreign Contribution Regulation Act [FRCA] Registered? Yes
FRCA Registartion Number: 136550211
HEMOPHILIA SOCIETY (LUCKNOW) NGO Organization Members
Name Designation Pan Aadhaar UMA KANT TANDON President Available Available VINAY MANCHANDA Secretary Available Available PRAMOD KUMAR PANDEY Treasurer Available Available ARUN KUMAR DWIVEDI Member Available Available RAM PRAKASH MAURYA Vice President Available Available RAJEEV KRISHNA TANDON Member Available Available RAKESH KUMAR GUPTA Member Available Available
HEMOPHILIA SOCIETY (LUCKNOW) Source Funds
Department Name Source Finacial Year Amount Sanctioned Purpose Not Specified Any Other 2015-2016 Not Specified No Govt Grant or Overseas Fund received during the year. Not Specified Any Other 2016-2017 Not Specified No Govt Grant or Overseas Fund received during the year. Not Specified Any Other 2017-2018 Not Specified No Govt Grant or Overseas Fund received during the year. Not Specified Any Other 2018-2019 Not Specified No Govt Grant or Overseas Fund received during the year.
HEMOPHILIA SOCIETY (LUCKNOW) Key Issues and
Operational Areas, Major Activiities & Achivements
Operational Districts: Lucknow
Operational States: UTTAR PRADESH
AchieveMents: Holding regular awareness and education camp, doing best efforts to ensure availability of anti hemophilia factors in Government hospitals for treatment of patients suffering with hemophilia disorder, providing financial and other assistance to poor hemophilic patients arranging and managing Hemophilia Treatment Centre where physiotherapy and counselling of hemophilic patients is done by Volunteers. Identifying more and more areas for the betterment and welfare of hemophilic patients.
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