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ABOUT THIS PAGE
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PharmaCompass offers a list of Dl-Threonine 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 Dl-Threonine manufacturer or Dl-Threonine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dl-Threonine manufacturer or Dl-Threonine supplier.
PharmaCompass also assists you with knowing the Dl-Threonine API Price utilized in the formulation of products. Dl-Threonine API Price is not always fixed or binding as the Dl-Threonine Price is obtained through a variety of data sources. The Dl-Threonine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 2-amino-3-hydroxy-butanoic acid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 2-amino-3-hydroxy-butanoic acid, including repackagers and relabelers. The FDA regulates 2-amino-3-hydroxy-butanoic acid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 2-amino-3-hydroxy-butanoic acid 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 2-amino-3-hydroxy-butanoic acid supplier is an individual or a company that provides 2-amino-3-hydroxy-butanoic acid active pharmaceutical ingredient (API) or 2-amino-3-hydroxy-butanoic acid finished formulations upon request. The 2-amino-3-hydroxy-butanoic acid suppliers may include 2-amino-3-hydroxy-butanoic acid API manufacturers, exporters, distributors and traders.
click here to find a list of 2-amino-3-hydroxy-butanoic acid suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A 2-amino-3-hydroxy-butanoic acid DMF (Drug Master File) is a document detailing the whole manufacturing process of 2-amino-3-hydroxy-butanoic acid active pharmaceutical ingredient (API) in detail. Different forms of 2-amino-3-hydroxy-butanoic acid DMFs exist exist since differing nations have different regulations, such as 2-amino-3-hydroxy-butanoic acid USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A 2-amino-3-hydroxy-butanoic acid DMF submitted to regulatory agencies in the US is known as a USDMF. 2-amino-3-hydroxy-butanoic acid USDMF includes data on 2-amino-3-hydroxy-butanoic acid's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 2-amino-3-hydroxy-butanoic acid USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of 2-amino-3-hydroxy-butanoic acid suppliers with USDMF on PharmaCompass.
2-amino-3-hydroxy-butanoic acid 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 2-amino-3-hydroxy-butanoic acid 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 2-amino-3-hydroxy-butanoic acid GMP manufacturer or 2-amino-3-hydroxy-butanoic acid GMP API supplier for your needs.
A 2-amino-3-hydroxy-butanoic acid CoA (Certificate of Analysis) is a formal document that attests to 2-amino-3-hydroxy-butanoic acid's compliance with 2-amino-3-hydroxy-butanoic acid specifications and serves as a tool for batch-level quality control.
2-amino-3-hydroxy-butanoic acid CoA mostly includes findings from lab analyses of a specific batch. For each 2-amino-3-hydroxy-butanoic acid 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.
2-amino-3-hydroxy-butanoic acid may be tested according to a variety of international standards, such as European Pharmacopoeia (2-amino-3-hydroxy-butanoic acid EP), 2-amino-3-hydroxy-butanoic acid JP (Japanese Pharmacopeia) and the US Pharmacopoeia (2-amino-3-hydroxy-butanoic acid USP).
