Simson Pharma is a major Indian exporter dealing with Certified Reference standards, Research chemicals, Metabolites, Isotope labelled compounds and Traceable working standards in The United States of America. Our speciality lies in developing custom synthesis of complex organic compounds and intermediates, reference compounds, custom peptide and amino acids.
All supplies to US pharma firms include production of APIs, Impurities, Metabolites and Stable Isotope Compounds. Our pioneering methodology has resulted in becoming reputed manufacturer of Complicated Impurity Standards. We are a highly reliable and complete solution provider in identifying, synthesizing and qualifying any Unknown Impurity.
For all verification and validation, we follow FDA and its Current Good Manufacturing Practice (CGMP) regulations. The CGMP regulations for drugs contain minimum requirements for the methods, facilities, and controls used in manufacturing, processing, and packing of a drug product. The regulations make sure that a product is safe for use, and that it has the ingredients and strength it claims to have. The pharmaceutical or drug quality-related regulations processes are adhered to.