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