Genetic & Molecular Testing Services at Individual and Population Level
- Patient Screening – Diagnosis of patients suffering from various genetic disorders like Sickle Cell Anaemia, Alpha and Beta Thalassemia, Spinal Muscular Atrophy, Duchenne Muscular Dystrophy etc.).
- Family and carrier screening for couples and families who are at the risk of the above genetic disorders
- Prenatal & Newborn Screening Tests – Preventing recurrence of genetic disorders and ensuring timely interventions.
- Customized Test Panels – Tailored molecular testing for specific community needs.
Preventive & Community Health Solutions
- Awareness & Screening programs – On-site testing for all individuals including tribal and rural communities.
- Genetic Counselling – Helping families understand results and make informed reproductive choices.
- Pre-Marital & Pre-Conception Screening – Preventing the transmission of genetic conditions.
Research & Development Services
- Conductance of research and develop diagnostic solutions for health problems
- Protocol Development – Simplified methods for low-resource labs and hospitals.
- Kit Development & Validation – Affordable and rapid molecular diagnostic kits.
Training & Capacity Building
- Hands-on Workshops – Training healthcare workers in molecular testing, molecular and cellular techniques.
- Skill Development – Building capacity for local labs to adopt robust diagnostic methods.
- Knowledge Sharing – Awareness programs/talks for medical and scientific professionals and communities.
Partnerships & Consultancy
- Hospital & NGO Partnerships – Extending affordable testing to underserved areas.
- Diagnostic Lab Consultancy – Helping labs set up and optimize molecular diagnostics.
- Public Health Programs – Supporting large-scale screening initiatives for genetic diseases.
- Projects/Grants Consultancy – Guidance on actionable goals, sustainability, budget, manpower planning, lab setup, and evaluation of feasibility/progress.
