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Experiments are designed to quantify its effects on collagen I and III synthesis (via qPCR or Western blot), myofibroblast differentiation (by measuring -smooth muscle actin expression), and the critical MMP/TIMP balance

The complete approval process consists of five major stages: preclinical toxicology studies, Phase I human safety and tolerance testing, Phase II efficacy evaluation, Phase III large-scale controlled clinical trials, and GMP manufacturing site audits

states and internationally, including Canada, Europe, Australia, and other regions

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Growth Monitoring Monitor growth signals such as headcount expansion, revenue trends, and market presence: Identify companies scaling rapidly or with potential to consolidate fragmented markets