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ABOUT THIS PAGE
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PharmaCompass offers a list of Levomefolate 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 Levomefolate manufacturer or Levomefolate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Levomefolate manufacturer or Levomefolate supplier.
PharmaCompass also assists you with knowing the Levomefolate API Price utilized in the formulation of products. Levomefolate API Price is not always fixed or binding as the Levomefolate Price is obtained through a variety of data sources. The Levomefolate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A L-methylfolate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of L-methylfolate, including repackagers and relabelers. The FDA regulates L-methylfolate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. L-methylfolate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of L-methylfolate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A L-methylfolate supplier is an individual or a company that provides L-methylfolate active pharmaceutical ingredient (API) or L-methylfolate finished formulations upon request. The L-methylfolate suppliers may include L-methylfolate API manufacturers, exporters, distributors and traders.
click here to find a list of L-methylfolate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
L-methylfolate 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-methylfolate 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-methylfolate GMP manufacturer or L-methylfolate GMP API supplier for your needs.
A L-methylfolate CoA (Certificate of Analysis) is a formal document that attests to L-methylfolate's compliance with L-methylfolate specifications and serves as a tool for batch-level quality control.
L-methylfolate CoA mostly includes findings from lab analyses of a specific batch. For each L-methylfolate 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-methylfolate may be tested according to a variety of international standards, such as European Pharmacopoeia (L-methylfolate EP), L-methylfolate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (L-methylfolate USP).
