Services

Carrier/Patient Screening – For couples and families at risk of genetic disorders (Spinal Muscular Atrophy, Muscular Dystrophies, Thalassemia, Sickle Cell Anaemia, etc.).
Prenatal & Newborn Screening Panel – Preventing recurrence of genetic disorders and ensuring timely interventions.
Customized Test Panels – Tailored molecular testing for specific community needs.

Awareness & Screening Camps – On-site testing in tribal and rural communities.
Genetic Counseling – Helping families understand results and make informed reproductive choices.
Pre-Marital & Pre-Conception Screening – Preventing the transmission of genetic conditions.

Kit Development & Validation – Affordable and rapid molecular diagnostic kits.
Protocol Development – Simplified methods for low-resource labs and hospitals.
State-of-the-Art Facilities – Access to advanced laboratory equipment (automatic DBS puncher, DNA extractor, molecular biology instruments) on a cost-sharing basis.
Research Data & Biobank Access – Database of patient/phenotype information (nutrition, anthropometry, cognition) plus access to blood, dried blood spot, and DNA samples for research/training.

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 professionals and communities.

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.