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Regulatory impact assessment (RIA) is an essential step for ensuring pharmaceutical product compliance, quality, and safety whenever changes occur in products or their manufacturing processes. However, this process has traditionally been complex and time-consuming, with risks of delaying product availability and increasing regulatory workload.. Today, Generative AI (GenAI) is rapidly changing this landscape, presenting new opportunities for efficiency and accuracy across global pharma operations....

It processes over one thousand interactions per week on cloud infrastructure, making high-precision ligand binding calculations available through a user-friendly interface.. How XFEP Works with High‑Precision Physics and AI‑Driven Modeling. Physics‑Driven Free Energy Perturbation Enables Accurate Binding Predictions...