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