About us
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About Us
Diverse technologies with global impact
Lightening Lives is a company that was started with a mission to create a global impact. Our focus is on developing accessible, affordable, and highly accurate diagnostic solutions that reach even the most underserved communities.
- Trusted expertise in molecular diagnostics and genetic screening
- Bringing affordable healthcare solutions to underserved communities
- Experienced professionals with a passion for improving lives
Founder
Dr. Giriraj Ratan Chandak
Dr Giriraj Ratan Chandak is a physician, scientist and a medical researcher with extensive expertise in molecular diagnostics and genetic disorders. He superannuated as a Chief Scientist from the CSIR-Centre for Cellular and Molecular Biology (CCMB), an autonomous institute par excellence where he made significant contributions to the understanding of genetic diseases. Dr Chandak has been one of the founding faculties of the Centre for DNA Fingerprinting and Diagnostics (CDFD) where he also served as the Director and is currently the Director of the Sickle Cell Anaemia-Elimination Mission, leading efforts to eradicate sickle cell anaemia in underserved populations. He is a Fellow of all four National Science Academies of India and a Fellow of The World Academy of Sciences, Italy along with the prestigious Sir J.C. Bose Fellowship for his groundbreaking work in genetic research. In addition to his academic and research achievements, Dr Chandak is actively involved in various consortiums and non-profit organizations focused on advancing healthcare and improving diagnostic access in resource-limited settings. He holds an extensive background in both clinical and research settings, with a focus on genetic disorders such as hemoglobinopathies and musculopathies. Driven by a passion for improving healthcare accessibility, Dr Chandak founded Lightening Lives LLP to develop cost-effective, efficient diagnostic tools that can transform patient care. His leadership and vision continue to guide the company’s mission to reduce disease burdens and improve health outcomes worldwide.
Co-Founder
Mrs. Nidhi Chandak
Nidhi, Co-Founder of Lightening Lives LLP, brings a strong academic foundation with an MSc in Operations Research and a Post Graduate Diploma in Computer Applications. Her expertise in statistical data management and operations optimization drives the company's mission of providing affordable and efficient diagnostic services to underserved populations, particularly those affected by musculopathies and hemoglobinopathies. With experience in interacting directly with patients, families, and support groups, Nidhi combines technical proficiency with a compassionate approach to healthcare.
Our Team
Our Team
Ms. Manisha Arumalla
Scientific Officer
Mr. Abhishek Chandak
Financial Consultant
Ms. Mehraj Begum
Admin and Operations Executive
Ms. Punyasri PSKDB
Technical Officer
Dr. Vivek Sharma
Chief Business & Strategy Advisor
Affordable & Innovative Diagnostic Solutions for All
Cutting-edge Genetic Tests
From carrier screening to newborn testing, we provide accurate, rapid, and low-cost molecular diagnostics tailored to community needs.
Innovative Diagnostic Kits
Our CSIR-SCAN, SickThal, and HemoSwift kits ensure faster, more reliable results—empowering labs, hospitals, and communities with accessible solutions.
Impact Stories From Lightening Lives
Each story reminds us why we began—every child’s smile, every family’s relief, and every life changed fills us with gratitude. At Lightening Lives, we are humbled to serve humanity by bringing hope where it’s needed the most through science and innovation.
In a small tribal village of Madhya Pradesh, a 3-year-old boy was showing signs of muscle weakness. His family had no access to specialized hospitals and assumed it was just a nutritional issue. Through an NGO, they came across Lightening Lives’s affordable molecular test, and he was quickly diagnosed with Duchenne Muscular Dystrophy (DMD). Timely diagnosis allowed the family to start supportive therapy early, join patient support groups, and prevent years of uncertainty. For the first time, they felt empowered with knowledge, not fear.
A tribal couple from Chhattisgarh lost their first child to Spinal Muscular Atrophy (SMA) without ever knowing the cause. When they approached us through a government screening platform, during their second pregnancy, we carried out carrier testing. Results showed both parents carried the SMA mutation. With genetic counseling and early testing, they made an informed decision that prevented the recurrence of this devastating disease. Today, they have a healthy child, and the couple often says—“We didn’t just save a child, we saved our family’s future.”
In a tribal hamlet of Odisha, a young couple came to us after noticing similar breathing difficulties, muscle weakness, severe anaemia and prolonged repeated infections in two children in their extended family. Our robust molecular testing revealed both were carriers of Sickle Cell Anaemia (SCA). With this knowledge, they were able to avoid passing the condition on to their children. This simple, quick test broke a generational cycle of suffering that the community thought was “fate.” For the first time, science brought hope.
A tribal mother in Jharkhand brought her 6-year-old daughter to a local health camp where we were conducting awareness and testing. The girl was diagnosed with DMD at an early stage. The mother also underwent carrier testing and was found positive. With this crucial knowledge, the family received counseling and could make informed choices for future pregnancies. They told us, “We never knew such testing existed for people like us. You have given us knowledge that will save our next child.”
Why Choose Us
Why you should choose Lightening Lives
At Lightening Lives, we are committed to delivering world-class diagnostic solutions that make a real difference in people’s lives. Our laboratory is built on innovation, compassion, and precision.
World-Class Diagnostics
We provide highly accurate and advanced diagnostic testing services using state-of-the-art technologies, ensuring reliable results that empower families.
Advanced Microscopy & Research
Our advanced microscopy and molecular research capabilities enable us to detect and study conditions with utmost precision, ensuring timely diagnosis.
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