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ABOUT THIS PAGE
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PharmaCompass offers a list of Surfadone LP-300 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 Surfadone LP-300 manufacturer or Surfadone LP-300 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Surfadone LP-300 manufacturer or Surfadone LP-300 supplier.
PharmaCompass also assists you with knowing the Surfadone LP-300 API Price utilized in the formulation of products. Surfadone LP-300 API Price is not always fixed or binding as the Surfadone LP-300 Price is obtained through a variety of data sources. The Surfadone LP-300 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 1-Dodecyl-2-pyrrolidinone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 1-Dodecyl-2-pyrrolidinone, including repackagers and relabelers. The FDA regulates 1-Dodecyl-2-pyrrolidinone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 1-Dodecyl-2-pyrrolidinone 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 1-Dodecyl-2-pyrrolidinone supplier is an individual or a company that provides 1-Dodecyl-2-pyrrolidinone active pharmaceutical ingredient (API) or 1-Dodecyl-2-pyrrolidinone finished formulations upon request. The 1-Dodecyl-2-pyrrolidinone suppliers may include 1-Dodecyl-2-pyrrolidinone API manufacturers, exporters, distributors and traders.
click here to find a list of 1-Dodecyl-2-pyrrolidinone suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A 1-Dodecyl-2-pyrrolidinone DMF (Drug Master File) is a document detailing the whole manufacturing process of 1-Dodecyl-2-pyrrolidinone active pharmaceutical ingredient (API) in detail. Different forms of 1-Dodecyl-2-pyrrolidinone DMFs exist exist since differing nations have different regulations, such as 1-Dodecyl-2-pyrrolidinone USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A 1-Dodecyl-2-pyrrolidinone DMF submitted to regulatory agencies in the US is known as a USDMF. 1-Dodecyl-2-pyrrolidinone USDMF includes data on 1-Dodecyl-2-pyrrolidinone's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 1-Dodecyl-2-pyrrolidinone USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of 1-Dodecyl-2-pyrrolidinone suppliers with USDMF on PharmaCompass.
1-Dodecyl-2-pyrrolidinone 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 1-Dodecyl-2-pyrrolidinone 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 1-Dodecyl-2-pyrrolidinone GMP manufacturer or 1-Dodecyl-2-pyrrolidinone GMP API supplier for your needs.
A 1-Dodecyl-2-pyrrolidinone CoA (Certificate of Analysis) is a formal document that attests to 1-Dodecyl-2-pyrrolidinone's compliance with 1-Dodecyl-2-pyrrolidinone specifications and serves as a tool for batch-level quality control.
1-Dodecyl-2-pyrrolidinone CoA mostly includes findings from lab analyses of a specific batch. For each 1-Dodecyl-2-pyrrolidinone 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.
1-Dodecyl-2-pyrrolidinone may be tested according to a variety of international standards, such as European Pharmacopoeia (1-Dodecyl-2-pyrrolidinone EP), 1-Dodecyl-2-pyrrolidinone JP (Japanese Pharmacopeia) and the US Pharmacopoeia (1-Dodecyl-2-pyrrolidinone USP).
