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PharmaCompass offers a list of Vinpocetine 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 Vinpocetine manufacturer or Vinpocetine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Vinpocetine manufacturer or Vinpocetine supplier.
PharmaCompass also assists you with knowing the Vinpocetine API Price utilized in the formulation of products. Vinpocetine API Price is not always fixed or binding as the Vinpocetine Price is obtained through a variety of data sources. The Vinpocetine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Vinpocetine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vinpocetine, including repackagers and relabelers. The FDA regulates Vinpocetine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vinpocetine 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 Vinpocetine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Vinpocetine supplier is an individual or a company that provides Vinpocetine active pharmaceutical ingredient (API) or Vinpocetine finished formulations upon request. The Vinpocetine suppliers may include Vinpocetine API manufacturers, exporters, distributors and traders.
click here to find a list of Vinpocetine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Vinpocetine DMF (Drug Master File) is a document detailing the whole manufacturing process of Vinpocetine active pharmaceutical ingredient (API) in detail. Different forms of Vinpocetine DMFs exist exist since differing nations have different regulations, such as Vinpocetine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Vinpocetine DMF submitted to regulatory agencies in the US is known as a USDMF. Vinpocetine USDMF includes data on Vinpocetine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Vinpocetine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Vinpocetine suppliers with USDMF on PharmaCompass.
A Vinpocetine CEP of the European Pharmacopoeia monograph is often referred to as a Vinpocetine Certificate of Suitability (COS). The purpose of a Vinpocetine CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Vinpocetine EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Vinpocetine to their clients by showing that a Vinpocetine CEP has been issued for it. The manufacturer submits a Vinpocetine CEP (COS) as part of the market authorization procedure, and it takes on the role of a Vinpocetine CEP holder for the record. Additionally, the data presented in the Vinpocetine CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Vinpocetine DMF.
A Vinpocetine CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Vinpocetine CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Vinpocetine suppliers with CEP (COS) on PharmaCompass.
A Vinpocetine written confirmation (Vinpocetine WC) is an official document issued by a regulatory agency to a Vinpocetine manufacturer, verifying that the manufacturing facility of a Vinpocetine active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Vinpocetine APIs or Vinpocetine finished pharmaceutical products to another nation, regulatory agencies frequently require a Vinpocetine WC (written confirmation) as part of the regulatory process.
click here to find a list of Vinpocetine suppliers with Written Confirmation (WC) on PharmaCompass.
Vinpocetine 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 Vinpocetine 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 Vinpocetine GMP manufacturer or Vinpocetine GMP API supplier for your needs.
A Vinpocetine CoA (Certificate of Analysis) is a formal document that attests to Vinpocetine's compliance with Vinpocetine specifications and serves as a tool for batch-level quality control.
Vinpocetine CoA mostly includes findings from lab analyses of a specific batch. For each Vinpocetine 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.
Vinpocetine may be tested according to a variety of international standards, such as European Pharmacopoeia (Vinpocetine EP), Vinpocetine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Vinpocetine USP).