Pharmaceutical Intermediates for Drug Development | High-Quality Solutions

Standards of pi (pharmaceutical ingredients) are strict guidelines that define quality, safety, and efficacy, and our company adheres to global standards of pi to deliver superior products. International standards of pi, such as those set by USP (United States Pharmacopeia), EP (European Pharmacopoeia), and BP (British Pharmacopoeia), specify requirements for purity, impurity limits, and testing methods. Standards of pi for APIs mandate purity levels of at least 98%, with strict limits on residual solvents (e.g., acetone <5000 ppm) and heavy metals (mercury <0.001 ppm). Standards of pi also cover physical properties like particle size and solubility, ensuring consistent performance in drug formulations. Our production processes are designed to meet these standards of pi, with in-house testing laboratories equipped to verify compliance through advanced techniques. By aligning with standards of pi, we ensure that our pharmaceutical ingredients integrate seamlessly into drug manufacturing, providing clients in America, Europe, and Southeast Asia with materials they can trust, making standards of pi the foundation of our product quality.