USP establishes written (documentary) and physical (reference) standards for medicines, food ingredients, dietary supplement products, and ingredients. These standards are used by regulatory agencies and manufacturers to help to ensure that these products are of the appropriate identity, as well as strength, quality, purity, and consistency. Prescription and over-the-counter medicines available in the United States must, by federal law, meet USP-NF public standards, where such standards exist. Many other countries use the USP-NF instead of issuing their own pharmacopeia, or to supplement their government pharmacopeia. USP is the most widely used reference standards in Bangladesh & We provide USP reference standards by taking order from our valued pharmaceutical clients. We maintain a very sound connection with the USP officials & that’s why our USP delivery is fast, safe, reliable and always comprised to match our commitment.
The European Pharmacopoeia (EDQM) is a major regional pharmacopoeia which provides common quality standards throughout the pharmaceutical industry in Europe to control the quality of medicines, and the substances used to manufacture them. Several legal texts make the European Pharmacopoeia mandatory in Europe. The Convention on the Elaboration of a European Pharmacopoeia which was adopted by the Council of Europe in 1964, laid the groundwork for the development of the European Pharmacopoeia. In 1994, a Protocol was adopted, amending the Convention to prepare for the accession of the European Union (EU), and defining the respective powers of the European Union and its Member States within the European Pharmacopoeia Commission. We provide EP reference standards by taking order from our valued pharmaceutical clients. Our delivery is fast, safe, reliable and always comprised to match our commitment.
The regulation of medicinal products by officials in the United Kingdom is managed by The British Pharmacopoeia. In this Pharmacopoeia, certain drugs and preparations are included regardless of the existence of actual or potential patent rights. Where substances are protected by letters patent, their inclusion in the Pharmacopoeia neither conveys, nor implies, license to manufacture. It is an annual published collection of quality standards for UK medicinal substances. It is used by individuals and organizations involved in pharmaceutical research, development, manufacture and testing. We provide BP reference standards by taking order from our valued pharmaceutical clients. Our delivery is fast, safe, reliable and always comprised to match our commitment.
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