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PharmaCompass offers a list of Vitamin K2 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 Vitamin K2 manufacturer or Vitamin K2 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Vitamin K2 manufacturer or Vitamin K2 supplier.
PharmaCompass also assists you with knowing the Vitamin K2 API Price utilized in the formulation of products. Vitamin K2 API Price is not always fixed or binding as the Vitamin K2 Price is obtained through a variety of data sources. The Vitamin K2 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Menatetrenone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Menatetrenone, including repackagers and relabelers. The FDA regulates Menatetrenone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Menatetrenone 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 Menatetrenone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Menatetrenone supplier is an individual or a company that provides Menatetrenone active pharmaceutical ingredient (API) or Menatetrenone finished formulations upon request. The Menatetrenone suppliers may include Menatetrenone API manufacturers, exporters, distributors and traders.
click here to find a list of Menatetrenone suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Menatetrenone DMF (Drug Master File) is a document detailing the whole manufacturing process of Menatetrenone active pharmaceutical ingredient (API) in detail. Different forms of Menatetrenone DMFs exist exist since differing nations have different regulations, such as Menatetrenone USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Menatetrenone DMF submitted to regulatory agencies in the US is known as a USDMF. Menatetrenone USDMF includes data on Menatetrenone's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Menatetrenone USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Menatetrenone suppliers with USDMF on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Menatetrenone Drug Master File in Japan (Menatetrenone JDMF) empowers Menatetrenone API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Menatetrenone JDMF during the approval evaluation for pharmaceutical products. At the time of Menatetrenone JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Menatetrenone suppliers with JDMF on PharmaCompass.
Menatetrenone 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 Menatetrenone 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 Menatetrenone GMP manufacturer or Menatetrenone GMP API supplier for your needs.
A Menatetrenone CoA (Certificate of Analysis) is a formal document that attests to Menatetrenone's compliance with Menatetrenone specifications and serves as a tool for batch-level quality control.
Menatetrenone CoA mostly includes findings from lab analyses of a specific batch. For each Menatetrenone 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.
Menatetrenone may be tested according to a variety of international standards, such as European Pharmacopoeia (Menatetrenone EP), Menatetrenone JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Menatetrenone USP).
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