Could you explain the full process of how the stem cells used in your treatments are sourced, processed, and prepared before they are administered to patients? I’m particularly interested in understanding whether the cells are autologous or donor-derived, how they’re handled in terms of sterilization, storage, and viability, and whether they are cultured or modified in any way. Additionally, what quality control protocols do you follow to ensure the stem cells meet safety and efficacy standards—such as screening for contamination, genetic stability, or cell potency? Knowing the scientific and regulatory steps behind the treatment would really help me feel confident in the safety and reliability of the procedure.