01 1Keshava Organics
01 1L-Selenomethionine (Selenomethionine) USP
01 1WC-0244
01 1India
L-Selenomethionine (Selenomethionine) USP
Date of Issue : 2022-12-09
Valid Till : 2025-07-02
Written Confirmation Number : WC-0244
Address of the Firm : Plot No. T-97 & 100, MIDC, Tarapur, -401 506, Taluka: Palghar, Dist-Thane Zone-4
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PharmaCompass also assists you with knowing the L-Selenomethionine API Price utilized in the formulation of products. L-Selenomethionine API Price is not always fixed or binding as the L-Selenomethionine Price is obtained through a variety of data sources. The L-Selenomethionine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A BioSel 5000 L-Selenomethionine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of BioSel 5000 L-Selenomethionine, including repackagers and relabelers. The FDA regulates BioSel 5000 L-Selenomethionine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. BioSel 5000 L-Selenomethionine API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A BioSel 5000 L-Selenomethionine supplier is an individual or a company that provides BioSel 5000 L-Selenomethionine active pharmaceutical ingredient (API) or BioSel 5000 L-Selenomethionine finished formulations upon request. The BioSel 5000 L-Selenomethionine suppliers may include BioSel 5000 L-Selenomethionine API manufacturers, exporters, distributors and traders.
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A BioSel 5000 L-Selenomethionine written confirmation (BioSel 5000 L-Selenomethionine WC) is an official document issued by a regulatory agency to a BioSel 5000 L-Selenomethionine manufacturer, verifying that the manufacturing facility of a BioSel 5000 L-Selenomethionine active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting BioSel 5000 L-Selenomethionine APIs or BioSel 5000 L-Selenomethionine finished pharmaceutical products to another nation, regulatory agencies frequently require a BioSel 5000 L-Selenomethionine WC (written confirmation) as part of the regulatory process.
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