About Us

 

The U.S. Food and Drug Administration (FDA) defines a reference-standard material as a “highly purified compound that is well characterized.”

The monitoring and regulation of pharmaceutical impurities is a critical issue facing the pharmaceutical industry across the globe. These impurities have an impact on the quality and safety of drugs; thereby making their detection and evaluation imperative in the development of new pharmaceutical products.

Nia innovation is a futuristic organisation that works with leading pharmaceutical companies to deliver high quality certified reference standards, impurity standards and degradation impurities to ensure accuracy and validity of analytical methods being used by our clients. Our USP is our belief in a customer centric model that works to deliver a competitive advantage to customers by matching our processes to their needs.

Organisational efficiency, quantitative synthesis capabilities , innovative abilities and prompt customer service marks the building blocks of our organisation. Contact us to know more.