Latest News & Media

Press Release

Sep 09,2025

Patient-centric nonprofit accelerates practical partnerships across borders to keep rare disease research…

Press Release

Mar 11,2025

Indo US Rare Disease Day at IndoUSrare – Bridging Nations, Empowering RARE Lives Combating Rare Diseases by Fostering Cross Border…

Press Release

Dec 04, 2024

The second annual Indo US Bridging RARE Summit received an overwhelming response from all stakeholders of rare…

Press Release

Press Release

Nov 05, 2024

The Indo US Bridging RARE Summit 2024 will spotlight the urgent need for cross-border collaborations to address…

Press Release

Press Release

Oct 11, 2024

Artificial intelligence (AI) and machine learning (ML) are poised to be play a pivotal role in clinical trials by automating patient recruitment…

Press Release

Feb 29, 2024

Indo US Organization for Rare Diseases (IndoUSrare) has always been a steadfast ally to rare disease patients, and Rare Disease Day 2024 will be no exception…

Articles

Feb 17, 2024

One of the main challenges in rare diseases is the unavailability of reliable estimates of prevalence and incidence. The lack of epidemiological data makes…

Articles

Jan 28, 2024

In the realm of clinical trials and rare disease research, the intersection of Artificial Intelligence (AI) and Machine Learning (ML) holds the promise of…

Press Release

Jan 3, 2024

In rare disease research, companies like IndoUSRare are exploring effective strategies such as establishing clinical research sites in countries with a higher…

Press Release

Nov 6, 2023

The FDA’s Commissioner, Dr. Robert M. Califf, recently visited India and shared his opinion on India’s Unique Opportunity and Important Responsibility as the…

Press Release

Oct 11, 2023

With an increasing number of U.S. biopharmaceutical firms feeling the financial constraints imposed by the Inflation Reduction Act (IRA) and subsequently…

Press Release

Sep 20, 2023

We all know AI (artificial intelligence) offers huge opportunities and huge risks for various industries, many of which we have discussed here on the blog. Today…

News

July 10, 2023

The World Health Organisation (WHO) defines rare diseases as debilitating, lifelong disorders with a prevalence of less than one per 1,000 persons. They include…

News

June 27, 2023

While attending the 2nd international conference on ALS/MND (Amyotrophic lateral sclerosis/Motor neuron disease), Dr Harsha Rajasimha stressed the need for…

Press Release

June 23, 2023

There is an urgent need for a patient registry for ALS and other rare diseases in India, said Dr Harsha Rajasimha, founder and executive chairman, Indo US…

News

June 05, 2023

Patients with rare diseases often lack adequate access to treatment due to a lack of awareness and medicines. Rare diseases include congenital malformations…

News

May 15, 2023

Join us for an enlightening episode of BioTalk with Rich Bendis as we explore the pivotal role of patient registries in rare disease research and treatment…

News

March 20, 2023

Global Registries Could Change the Lives of Hundreds of Millions of Rare Disease Patients Everywhere

Clinical trials and effective treatment protocols rely on comprehensive data on rare disease demographics and treatments. Rare diseases affect hundreds…

News

January 23, 2023

Restricted cross-border collaborations among governments, biotech companies and scientists severely curb the speed at which treatments for rare diseases…

News

February 22, 2022

February 28 marks International Rare Disease Day. While many improvements have been made in clinical trials for rare diseases, the drug development process…

Press Release

September 06, 2022

Political conflicts have stagnated the FDA’s attempts to modernize clinical trials to effectively reflect the global population. Research for rare disease treatments…

Press Release

October 17, 2022

New studies highlight the devastating economic burden of rare diseases. Impacting about 30 million people in the United States alone, the direct and indirect…

Press Release

December 12, 2022

New studies highlight the devastating economic burden of rare diseases. Impacting about 30 million people in the United States alone, the direct and indirect…

Press Release

December 12, 2022

Political conflicts have stagnated the FDA’s attempts to modernize clinical trials to effectively reflect the global population. Research for rare disease treatments…

Press Release

October 17, 2022

New studies highlight the devastating economic burden of rare diseases. Impacting about 30 million people in the United States alone, the direct and indirect…

News

June 22, 2022

We are happy to announce that IndoUSrare is a recipient of the Financial Advocacy in RARE Impact Grant sponsored by GlobalGenes…

News

May 15, 2023

Join us for an enlightening episode of BioTalk with Rich Bendis as we explore the pivotal role of patient registries in rare disease research and treatment…

blogs

March 26, 2021

Data is the new oil. The advancements in AI, data mining, big-data present enormous opportunities to build an open data ecosystem in healthcare to accelerate…

News

August 31, 2020

Harsha Rajasimha’s first encounter with rare disease came in 2009 as a genomics data scientist working with the National Institutes of Health’s National Eye…

News

April 20, 2021

IndoUSrare and RARE-X partnered to understand India’s rare disease landscape and conducted a feasibility study to determine the challenges to creating…

Press Release

August 13, 2014

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News

BioBuzz recently sat down for a conversation with Dr. Harsha K. Rajasimha, a leading rare disease advocate, the founder of the non-profit, IndoUSrare…

News

February 6, 2020

My first encounter with a rare disease was about 10 years ago at the neurobiology, neurodegeneration, and repair laboratory (NNRL Chief: Anand Swaroop) at the..

News

January 3, 2020

Hi, I am Harsha Rajasimha, Founder and Chairman of IndoUSrare, an independent non-profit organization focused on helping patients with rare diseases of Indian…

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