Chemicea is ISO 9001:2015, ISO 17034: 2016, ISO 17025:2017 and GMP certified company. A leading manufacturer of pharmaceutical reference standards. From the last 7 years we are serving to 500+ customers in 35+ countries in the world
We have best in class R and D facility of 3000 sq. ft. area. With a strong emphasis on quality and compliance we specialize in producing pharmaceutical products that meet the highest industry standards. Our state-of-the-art facilities and dedicated team of experts ensure that every product
We manufacture is of the utmost quality, adhering to stringent regulatory requirements.
A pharmaceutical reference standard is a substance or material that has been thoroughly characterized and established as a standard of identity, purity, potency, and other critical attributes.
Impurity standards in the pharmaceutical industry refer to reference materials or substances that are used to identify, quantify, and characterize impurities present in pharmaceutical products.
Working Standard is Drug substance or any other Chemical in the pharmaceutical industry is called as working standard or secondary standard or a working reference standard
Lorem Ipsum is simply dummy text of the printing and typesetting industry. Lorem Ipsum has been the industry's standard dummy text ever since the 1500s, when an unknown printer took a galley of type and scrambled it to make a type specimen book.
A metabolite is the intermediate end product of metabolism. The term metabolite is usually restricted to small molecules. A drug metabolite is a byproduct of break down, or “metabolizing,” a drug into a different substance.
At Chemicea, we are proud to offer a comprehensive range of services tailored to meet the diverse needs of the pharmaceuticals, research industries and research institutes
Building strong relationships, supplying quality products and surpassing client expectations have been the key drivers for us.
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