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