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    • Medicinal therapy
    • Nutritional therapy
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    • Medicinal Therapy

      • Tyrosinemia
      • Brunity


    • Nutritional Therapy

      • Phenylketonuria
      • PKU A formula
      • PKU B formula
      • PKU B (concentrate)
      • PKU express15 & 20
      • PKU express15 plus & 20 plus
      • Tyrosinemia
      • TYRo A Formula
      • TYR explore5
      • TYR gel
      • TYRo B Formula
      • TYR cooler15
      • TYR express plus 15 and 20
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Raising awareness and generating change for 300 million people worldwide living with rare diseases. We are 38 years old growing pharmaceutical conglomerate serving as a reliable partner.

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A ray of hope for better life and brighter future..

Empowering individuals with rare diseases through innovative medicinal & nutritional therapies and dedicated support, unlocking hope for brighter futures..

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Curing rare diseases

Rare diseases are health conditions that affect a small number of people compared to other prevalent diseases in the general population. The field of rare diseases is complex, heterogeneous, and continuously evolving. WHO defines rare disease as often debilitating lifelong disease or disorder with a prevalence of 1 or less, per 1000 population.

Sick Child
Mother
Check temprature
M+

Individuals globally suffer from Rare Diseases

K+

Total number of Rare Diseases Globally

M+

Total number of Individuals affected with Rare Diseases in India

Centres of Excellence (CoEs) for Rare Diseases

+

Identified Rare Diseases in India

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Challenges

Unavailability of medicines on time

The challenges posed by rare diseases in India include difficulty in collecting epidemiological data, making correct and timely diagnosis, complex tertiary level management involving long term care and rehabilitation, and unavailability of medicines and it’s prohibitive cost of treatment. Thus, making medicine available, accessible, and affordable for rare diseases is a significant challenge.

Why Brawn Rare Disease

Availability and accessibility to medicines and nutritional supplements are important to reduce morbidity and mortality associated with rare diseases. Besides the challenge of being unavailable, in many cases, the cost of these therapies if available can be prohibitively expensive, placing immense strain on healthcare resources. As government has begun a 'Make in India' initiative, with the primary objective of research and development of robust manufacturing facilities to reduce down on cost, Brawn’s parallel efforts are to collaborate with our global partners to reduce the therapy gap to make the medicines and supplements for rare diseases more easily available, accessible, and affordable to the affected families.

Available
Available

With a PAN India network at your disposal, help is never far away, ensuring timely access to essential resources and services wherever you are

Accessible

With our expansive team dedicated to assisting patients, accessibility to support and guidance is just a call or click away

Affordable

Our state-of-the-art manufacturing processes and strategic partnerships ensure cost-effective solutions without compromising on quality

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Our Aim and Commitment

To create a meaningful impact by offering Medicines & Food for Special Medical Purposes (FSMP) to those who need it the most.

To ensure the Medicines and Food for Special Medical Purposes (FSMP) is easily available, accessible and affordable for Indian masses suffering from rare diseases.

Heart Shape

Therapy focus

We are committed to collaborate and develop innovative and effective solutions for rare diseases.

Our therapeutic portfolio consists of a range of medicinal and nutritional products that address the specific needs and challenges of patients with rare conditions. Our products are based on cutting-edge research and clinical trials, and are designed to improve the quality of life and health outcomes of our patients. Whether, it is a novel drug or a dietary supplement, our portfolio offers a holistic and personalized approach to rare disease management.

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News articles

Explore our strategic alliances, upcoming events, and cutting-edge developments, all aimed at empowering those affected by rare diseases.

Discover our network of partnerships, upcoming events, and pioneering advancements, all dedicated to empowering individuals impacted by rare diseases. Join us as we forge alliances, host transformative events, and pioneer breakthroughs to support those navigating the challenges of rare conditions.

24 Aug 2024

Phenylketonuria - PMC (nih.gov)

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24 Aug 2024

Alkaptonuria: Current Perspectives - PMC (nih.gov)

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24 Aug 2024

Outcome of Tyrosinemia Type 1 in Indian Children

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Team

Partner with us

Collaboration is the core of what we do. Driven by empathy, compassion and tireless innovation, we bring together leading talent to create life-saving therapies for patients and their families.

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