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