Advanced Cell Processing Cleanrooms
The clinical success and safety of cellular therapies hinge fundamentally on processing protocols. Our partner laboratories operate strictly under international current Good Manufacturing Practice (cGMP) regulations. Every cellular unit—whether autologous bone marrow-derived, adipose-derived, or certified Wharton's Jelly MSC—is isolated, characterized, and tested in sterile laminar airflow cabinets.
Quality Control & Release Testing
- Flow Cytometry Surface Marker Verification: MSC confirmation via positive CD73, CD90, CD105 markers and negative CD34, CD45, HLA-DR expression.
- Microbial Sterility Screening: 14-day automated blood culture testing for aerobic, anaerobic bacteria, and fungi prior to release.
- Endotoxin & Mycoplasma Testing: LAL assay testing ensuring endotoxin concentrations remain below strict pharmacopeial thresholds (< 0.25 EU/ml).
- Cell Count & Viability Analysis: Automated acridine orange/propidium iodide (AO/PI) fluorescence quantification ensuring >90% living cells.
Virtual Tour of Partner Laboratories
State-of-the-art biological safety cabinets, cryopreservation storage, and surgical delivery theaters across our Delhi, Mumbai, and Bangalore centers.
Partner Hospital Network
International patients are admitted exclusively to multi-specialty tertiary care hospitals equipped with high-dependency units (HDU), intensive care suites (ICU), advanced neuro-imaging (3T MRI, PET-CT), and comfortable private deluxe inpatient accommodations featuring complimentary companion stays, high-speed Wi-Fi, and international catering options.