Welcome to Standalix, your premier destination for superior API impurity standards and quality control chemicals in Europe. With a steadfast commitment to excellence, we strive to be your reliable partner in ensuring the highest standards for research and quality control.
At Standalix, our vision is centered on elevating the standards of quality control within pharmaceutical companies. We are dedicated to providing exceptional support to quality control labs by offering precise, top-tier API impurity standards. Our aim is to empower these labs with the necessary tools and solutions to ensure uncompromising quality in pharmaceutical production.
We envision a landscape where quality control labs operate at the pinnacle of excellence, equipped with the most reliable quality standards provided by Standalix.
Our mission is to be the ultimate source for API impurity standards, providing uncompromising quality that meets the standards of the pharmaceutical industry. We aim to serve as a reliable, cost-affordable solution, ensuring that scientists and quality control departments have easy access to the most precise tools required for their research and quality assurance endeavors.
At Standalix, we believe that precision, trust, and availability are essential pillars in pharmaceutical research and quality assurance. Our philosophy is simple:
Help our clients accelerate drug development and safeguard patient safety by ensuring fast, reliable and access to a wide catalogue of the impurity standards they need.
We understand the complexity behind sourcing reference materials—especially when they’re rare, novel, or highly specific. That’s why we go beyond being just a supplier. We act as a partner, combining scientific expertise, regulatory know-how, and a vast global sourcing network to deliver high-purity standards that meet real-world demands.
At Standalix, we value both superior quality and cost-effectiveness, understanding the pivotal role API impurity standards play within pharmaceutical research and quality control. Our dedication extends beyond providing top-tier products. We are committed to ensuring that our offerings not only meet but exceed the standards set by the pharmaceutical industry.
We recognize that quality control departments within pharmaceutical companies rely not only on the excellence of the products but also on the associated documentation for thorough assessment and compliance. At Standalix, we prioritize the delivery of API impurity standards accompanied always by comprehensive Certificate of Analysis (COA) and Safety Data Sheets (SDS), as well as any other on-demand required documentation
Our aim is to support pharmaceutical quality control departments by providing more than just exceptional products. We seek to streamline their operations by delivering API impurity standards with the best service and integration with pharmaceutical IT systems/ERP. Our commitment to supreme quality at accessible prices, combined with comprehensive documentation, serves as the cornerstone for ensuring compliance and operational clarity within these critical departments.
