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REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
A 2-Deoxy-D-Glucose manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 2-Deoxy-D-Glucose, including repackagers and relabelers. The FDA regulates 2-Deoxy-D-Glucose manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 2-Deoxy-D-Glucose 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 2-Deoxy-D-Glucose manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 2-Deoxy-D-Glucose supplier is an individual or a company that provides 2-Deoxy-D-Glucose active pharmaceutical ingredient (API) or 2-Deoxy-D-Glucose finished formulations upon request. The 2-Deoxy-D-Glucose suppliers may include 2-Deoxy-D-Glucose API manufacturers, exporters, distributors and traders.
click here to find a list of 2-Deoxy-D-Glucose suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A 2-Deoxy-D-Glucose DMF (Drug Master File) is a document detailing the whole manufacturing process of 2-Deoxy-D-Glucose active pharmaceutical ingredient (API) in detail. Different forms of 2-Deoxy-D-Glucose DMFs exist exist since differing nations have different regulations, such as 2-Deoxy-D-Glucose USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A 2-Deoxy-D-Glucose DMF submitted to regulatory agencies in the US is known as a USDMF. 2-Deoxy-D-Glucose USDMF includes data on 2-Deoxy-D-Glucose's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 2-Deoxy-D-Glucose USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of 2-Deoxy-D-Glucose suppliers with USDMF on PharmaCompass.
2-Deoxy-D-Glucose 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 2-Deoxy-D-Glucose 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 2-Deoxy-D-Glucose GMP manufacturer or 2-Deoxy-D-Glucose GMP API supplier for your needs.
A 2-Deoxy-D-Glucose CoA (Certificate of Analysis) is a formal document that attests to 2-Deoxy-D-Glucose's compliance with 2-Deoxy-D-Glucose specifications and serves as a tool for batch-level quality control.
2-Deoxy-D-Glucose CoA mostly includes findings from lab analyses of a specific batch. For each 2-Deoxy-D-Glucose 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.
2-Deoxy-D-Glucose may be tested according to a variety of international standards, such as European Pharmacopoeia (2-Deoxy-D-Glucose EP), 2-Deoxy-D-Glucose JP (Japanese Pharmacopeia) and the US Pharmacopoeia (2-Deoxy-D-Glucose USP).
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