Brawn Laboratories Limited

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Brawn Laboratories Limited

Brawn has 38 years of legacy. Herbal division provides natural herbal solutions to all your problems. Founded by Mr.

Today we are among the fastest growing Pharma Indian multinationals, Brawn has grown exponentially in the last decade and made a distinct presence across the globe with its quality products. It makes me really proud to share the news of our upcoming US FDA and EU GMP-compliant plant at Halol, Gujarat. This will further boost our production capacities to serve humanity. With a renewed and strategic focus on R&D, the company has recently ventured into an exclusive R&D setup for API and Formulations conforming to international standards. The DSIR-approved facility has highly skilled scientists and doctors working on new generation molecules and innovative products, especially in the Oncology field. Brawn Cosmetics & Herbals (Herbal health care division) is a new age Herbals and Ayurvedic Product Company that strives to bring the traditional, time-tested goodness of Ayurveda with the blend of science and technology to 21st-century customers. Brij Raj Gupta, with a vision to provide the best quality Ayurvedic/Herbal products across the globe, the company has its own cGMP certified manufacturing unit based at Gurugram, Haryana. We are focused on developing new herbal products backed by scientific research and maintaining the purity of nature & safety without compromising the quality. At the same time, we are ambitious to find out the new panacea for people's healthier & beautiful life. Brawn has its’ presence in more than 60+ countries across South East Asia, Africa, Latin America, and CIS regions. Mission: To be among the top research-based global Ayurveda healthcare corporation through regulatory compliance and operational excellence offering quality products that are a true blend of ancient Ayurveda and modern technology. Vision: To develop and market affordable research-based quality herbal formulations to nurture the better life of people all across the globe.

22/11/2025

Every symptom tells a story. Every voice builds awareness. Alkaptonuria affects 1 in 250,000—let’s make those voices heard.

15/11/2025

Awareness: The First Prescription in Rare Disease Care
300 million lives. 7,000 diseases. One common challenge — being unseen.

Every rare disease may touch only a few lives, but together, they impact millions across the world.

Awareness is where change begins.
It leads to:

🕊️ Earlier diagnosis and timely medical care
💊 Access to the right treatment and patient support
🔬 Fuel for research and innovation
🧭 Informed health policies that drive real change
💞 Connected, stigma-free communities that care

Be the voice for the unseen.
Learn. Share. Support. Advocate.
Together, we turn awareness into care.

08/11/2025

🌍 Rare doesn’t mean alone.

Over 7,000 rare diseases affect more than 300 million people worldwide, yet many remain misunderstood.

Let’s replace myths with facts. Early diagnosis, research, and compassion can transform lives.

Together, we can ensure no patient is left behind. 💙

🌐https://brawnraredisease.in

01/11/2025

Rare Does Not Mean Small
Across the world, over 7,000 rare diseases exist ,together impacting more than 300 million lives.
In India alone, nearly 96 million people live with a rare disease.
Each condition may be rare, but together they are many.

Early diagnosis, awareness, and compassion can change lives.
Let’s make the invisible - visible.
Because every life matters.

12/10/2025

Why Rare Diseases Matter?

1. Hidden Burden:
Mostly genetic, progressive, and life-threatening - often affecting children and creating lifelong emotional and financial strain.

2. Diagnostic Odyssey:
Patients wait 5–7 years for a correct diagnosis after multiple hospital visits and tests.

3. Limited Treatment:
Out of 7,000+ rare diseases, less than 5% have approved therapies - many are costly or unavailable in India.

4. Economic Impact:
Families exhaust savings on care, adding hidden pressure to the national healthcare system.

5. Innovation Opportunity:
Addressing rare diseases can accelerate advances in genomics, personalized medicine, and digital diagnostics.

30/09/2025

✨ Rare disease care in India is getting stronger!
With 14 Centers of Excellence now under NPRD 2021 (including AIIMS Patna & RIMS Imphal), patients have better access to diagnosis, treatment & support. 💡
A step closer to healthcare where no one is left behind. 🌍💙

24/09/2025

Newborn Screening (NBS) is a life-saving tool that helps identify serious health conditions in infants at the earliest stage — enabling timely intervention and better long-term outcomes.

In India, NBS is not yet mandatory at the national level, though states like Goa have successfully implemented programs. Currently, the most commonly recommended and screened conditions include:
• Congenital Hypothyroidism (CH)
• Congenital Adrenal Hyperplasia (CAH)
• Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency

These conditions are prioritized due to their relatively high prevalence and the transformative health benefits of early detection.

Expanding awareness, accessibility, and policy adoption for Newborn Screening can truly shape healthier beginnings and a brighter future for every child in India.

19/09/2025

Tyrosinemia is a rare inherited disorder affecting the breakdown of the amino acid tyrosine.

If untreated, it leads to the buildup of toxic substances in the liver, kidneys, and other organs, causing serious health issues, especially in infants and young children.

Early diagnosis and medical management are crucial for a healthy future.

13/08/2025

PKU can be managed with a special low-protein diet, supplements, and regular checkups. Early newborn screening makes a big difference.

Hope begins with awareness.

26/07/2025

Children with PKU cannot process phenylalanine, an amino acid found in high-protein foods. If unmanaged, it can cause brain damage and learning difficulties. But with early detection, life can be normal.

19/07/2025

Phenylketonuria (PKU) is a rare genetic condition caused by inheriting two faulty PAH genes. Most parents are unaware
they’re carriers. It’s not your fault—it’s inherited. Early awareness can save lives.

📌 Let’s raise awareness about rare genetic conditions like PKU.

Address

Brawn Laboratories Ltd. , Plot No. 30, Opp. Infocity Tech Park-2, Sec/33
Gurugram
122001

Telephone

+919821192406

Website

https://brawnherbals.com/, https://brawnlabs.com/

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