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PharmaCompass offers a list of N-Vinyl-2-Pyrrolidone 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 N-Vinyl-2-Pyrrolidone manufacturer or N-Vinyl-2-Pyrrolidone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred N-Vinyl-2-Pyrrolidone manufacturer or N-Vinyl-2-Pyrrolidone supplier.
PharmaCompass also assists you with knowing the N-Vinyl-2-Pyrrolidone API Price utilized in the formulation of products. N-Vinyl-2-Pyrrolidone API Price is not always fixed or binding as the N-Vinyl-2-Pyrrolidone Price is obtained through a variety of data sources. The N-Vinyl-2-Pyrrolidone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A N-Vinyl-2-Pyrrolidone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of N-Vinyl-2-Pyrrolidone, including repackagers and relabelers. The FDA regulates N-Vinyl-2-Pyrrolidone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. N-Vinyl-2-Pyrrolidone 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 N-Vinyl-2-Pyrrolidone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A N-Vinyl-2-Pyrrolidone supplier is an individual or a company that provides N-Vinyl-2-Pyrrolidone active pharmaceutical ingredient (API) or N-Vinyl-2-Pyrrolidone finished formulations upon request. The N-Vinyl-2-Pyrrolidone suppliers may include N-Vinyl-2-Pyrrolidone API manufacturers, exporters, distributors and traders.
click here to find a list of N-Vinyl-2-Pyrrolidone suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A N-Vinyl-2-Pyrrolidone DMF (Drug Master File) is a document detailing the whole manufacturing process of N-Vinyl-2-Pyrrolidone active pharmaceutical ingredient (API) in detail. Different forms of N-Vinyl-2-Pyrrolidone DMFs exist exist since differing nations have different regulations, such as N-Vinyl-2-Pyrrolidone USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A N-Vinyl-2-Pyrrolidone DMF submitted to regulatory agencies in the US is known as a USDMF. N-Vinyl-2-Pyrrolidone USDMF includes data on N-Vinyl-2-Pyrrolidone's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The N-Vinyl-2-Pyrrolidone USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of N-Vinyl-2-Pyrrolidone suppliers with USDMF on PharmaCompass.
A N-Vinyl-2-Pyrrolidone CEP of the European Pharmacopoeia monograph is often referred to as a N-Vinyl-2-Pyrrolidone Certificate of Suitability (COS). The purpose of a N-Vinyl-2-Pyrrolidone CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of N-Vinyl-2-Pyrrolidone EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of N-Vinyl-2-Pyrrolidone to their clients by showing that a N-Vinyl-2-Pyrrolidone CEP has been issued for it. The manufacturer submits a N-Vinyl-2-Pyrrolidone CEP (COS) as part of the market authorization procedure, and it takes on the role of a N-Vinyl-2-Pyrrolidone CEP holder for the record. Additionally, the data presented in the N-Vinyl-2-Pyrrolidone CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the N-Vinyl-2-Pyrrolidone DMF.
A N-Vinyl-2-Pyrrolidone CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. N-Vinyl-2-Pyrrolidone 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 N-Vinyl-2-Pyrrolidone suppliers with CEP (COS) on PharmaCompass.
N-Vinyl-2-Pyrrolidone 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 N-Vinyl-2-Pyrrolidone 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 N-Vinyl-2-Pyrrolidone GMP manufacturer or N-Vinyl-2-Pyrrolidone GMP API supplier for your needs.
A N-Vinyl-2-Pyrrolidone CoA (Certificate of Analysis) is a formal document that attests to N-Vinyl-2-Pyrrolidone's compliance with N-Vinyl-2-Pyrrolidone specifications and serves as a tool for batch-level quality control.
N-Vinyl-2-Pyrrolidone CoA mostly includes findings from lab analyses of a specific batch. For each N-Vinyl-2-Pyrrolidone 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.
N-Vinyl-2-Pyrrolidone may be tested according to a variety of international standards, such as European Pharmacopoeia (N-Vinyl-2-Pyrrolidone EP), N-Vinyl-2-Pyrrolidone JP (Japanese Pharmacopeia) and the US Pharmacopoeia (N-Vinyl-2-Pyrrolidone USP).