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PharmaCompass offers a list of L-Methionine Sulfoximine API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right L-Methionine Sulfoximine manufacturer or L-Methionine Sulfoximine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred L-Methionine Sulfoximine manufacturer or L-Methionine Sulfoximine supplier.
PharmaCompass also assists you with knowing the L-Methionine Sulfoximine API Price utilized in the formulation of products. L-Methionine Sulfoximine API Price is not always fixed or binding as the L-Methionine Sulfoximine Price is obtained through a variety of data sources. The L-Methionine Sulfoximine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A L-Methionine Sulfoximine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of L-Methionine Sulfoximine, including repackagers and relabelers. The FDA regulates L-Methionine Sulfoximine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. L-Methionine Sulfoximine API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A L-Methionine Sulfoximine supplier is an individual or a company that provides L-Methionine Sulfoximine active pharmaceutical ingredient (API) or L-Methionine Sulfoximine finished formulations upon request. The L-Methionine Sulfoximine suppliers may include L-Methionine Sulfoximine API manufacturers, exporters, distributors and traders.
click here to find a list of L-Methionine Sulfoximine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A L-Methionine Sulfoximine DMF (Drug Master File) is a document detailing the whole manufacturing process of L-Methionine Sulfoximine active pharmaceutical ingredient (API) in detail. Different forms of L-Methionine Sulfoximine DMFs exist exist since differing nations have different regulations, such as L-Methionine Sulfoximine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A L-Methionine Sulfoximine DMF submitted to regulatory agencies in the US is known as a USDMF. L-Methionine Sulfoximine USDMF includes data on L-Methionine Sulfoximine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The L-Methionine Sulfoximine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of L-Methionine Sulfoximine suppliers with USDMF on PharmaCompass.
L-Methionine Sulfoximine Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.
GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).
PharmaCompass offers a list of L-Methionine Sulfoximine GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right L-Methionine Sulfoximine GMP manufacturer or L-Methionine Sulfoximine GMP API supplier for your needs.
A L-Methionine Sulfoximine CoA (Certificate of Analysis) is a formal document that attests to L-Methionine Sulfoximine's compliance with L-Methionine Sulfoximine specifications and serves as a tool for batch-level quality control.
L-Methionine Sulfoximine CoA mostly includes findings from lab analyses of a specific batch. For each L-Methionine Sulfoximine CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.
L-Methionine Sulfoximine may be tested according to a variety of international standards, such as European Pharmacopoeia (L-Methionine Sulfoximine EP), L-Methionine Sulfoximine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (L-Methionine Sulfoximine USP).
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