GLP Pharma Standards is a research-based global pharmaceutical company with a diverse combination of skills, resources and capabilities that provides a perfect platform to perform effectively in today's rapidly changing healthcare environment.
GLP Pharma Standards is the leading manufacturer and supplier of high quality API Impurities, Nitroso Impurities, Drug working standards, Drug Impurity Standards, Drug Metabolites, Genotoxic Impurities and Stable Isotope Labelled Compounds. We are the front runner in manufacturing of complicated Drug impurity standards.
We supply our wide range of products to our clients with all required analytical supporting data like CoA, NMR, C13, MASS, HPLC/GC, IR, TGA etc.
GLP Pharma Standards has been offering its services in the pharmaceutical impurities sector for the past decade by fulfilling the clients requirements all over the world.
GLP Pharma Standards is an ISO 9001:2015, ISO 17034:2016 certified company.
We are the complete solution provider in identifying, synthesizing and qualifying any Unknown impurities, without compromising on the quality of the products.
GLP Pharma Standards not only synthesize and supply molecules but also provides cost effective & innovative approach to help companies achieve success. We work closely with our clients for understanding their requirements and offer them time bound solutions. GLP Pharma is one stop solutions for Chemical development, Formulation development, Analytical development and for Regulatory services.
To sum-up GLP Pharma Standards is a Perfect choice for high quality Pharmaceutical Impurities, API related compounds, Intermediates, Metabolites, Drug Working Standards, Drug Impurity Standards, and Stable Isotope Labelled compounds.
Our Tenets: Highest Quality & Integrity