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