We apply advanced statistical models to interpret complex datasets. From chromatography results to genomic sequencing, we ensure accurate data translation to support your R&D objectives and regulatory submissions.

We consult on the design of in silico, in vitro, and in vivo trials. We map safe dose-response curves using regression formulas where the toxicity index LD50 is calculated with scientific precision to meet strict BPOM or FDA criteria.

Our seasoned scientists provide strategic advisory services for your projects. We help in protocol optimization, experimental design, and troubleshooting to ensure scientific validity and accelerated project timelines.

We run quantitative feasibility analyses to identify yield-to-cost ratios and ensure target purity. Furthermore, we structure optimal pathways—including Licensing, Joint Ventures, or Spin-offs—to extract maximum revenue from your R&D assets.

We audit biochemical data to draft technically bulletproof patent claims. We protect and license your proprietary methods—such as green extraction configurations—aligning with global Patent Cooperation Treaty (PCT) standards.

We bridge the gap between innovation and compliance. Our team assists in resolving non-conformities and aligning QA/QC protocols with international ISO, BPOM, and FDA standards to secure your manufacturing processes.