Screening is one of the most significant factors in prevention of non-communicable diseases as well as rare diseases.
RADOIR and IUMS IN Scientific Collaboration
In order to expand scientific, training and research collaboration, exchanging facilities, information and data mining capacity, RADOIR and IUMS signed a collaborative partnership MOU on Monday Jan. 21, 2019.
RADOIR and TUMS Scientific in Collaborative Partnership
In order to establish R & D collaborative committee on the scientific research prioritizations for the rare patients’ needs, a meeting session was held together with RADOIR & TUMS authorities.
RADOIR & ROYAN Institute Begin Their Collaborative Partnership
Rare Diseases Foundation of Iran and ROYAN Institute held a meeting session on the means of scientific research collaboration in the field of rare diseases and genetic disorders on Wednesday 2nd Jan, 2019.
National Strategic Plan Complication for Rare Diseases by RADOIR
Health socialization & social responsibility on health care system is the main topic of discussions during Dr.Hashemi’s ministership which was completely changed through emphasizing on NGOs’ impressive role, accordingly.
RADOIR at Hypophysis Diseases, Growth Hormone Disorder in Scientific Conference
The 7th Scientific Conference of Hypothesis Diseases, Growth Hormone Disorder in children and Adults was held on 21 December 2018 by the scientific secretary, Dr. Mohammad Khamseh and the executive secretory, Dr. Mojtaba Malek from Endocrine and Metabolism Institute of Iran Medical Science University at Parsian Evin hotel, Kooh-e-Noor hall.
RADOIR Membership at ICOSEP
Countersigned b/w RADOIR and Medical Science Faculty of Tehran University
A Memorandum of Understanding has been countersigned between RADOIR and Medical Science Faculty of Tehran University for Research & Scientific collaboration
Children with Rare Diseases at the First Joy Campaign of RADOIR
The first Joy “Campaign of RADOIR” with the slogan “Rare but not Alone!” held on 10th Dec, 2018 with the presence of some Comedians, storytellers, children’s favorite show men and clowns.
RADOIR at International Epigenetics & Epitranscriptomics Conference
Scientific board of Rare Diseases Foundation of Iran joined 2018 Int’l Epigenetics & Epitranscriptomics Conference which was held during November 26-27 in Helsinki-Finland at which RADOIR was one of the main collaborators.