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PharmaCompass offers a list of Histidine Dihydrochloride 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 Histidine Dihydrochloride manufacturer or Histidine Dihydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Histidine Dihydrochloride manufacturer or Histidine Dihydrochloride supplier.
PharmaCompass also assists you with knowing the Histidine Dihydrochloride API Price utilized in the formulation of products. Histidine Dihydrochloride API Price is not always fixed or binding as the Histidine Dihydrochloride Price is obtained through a variety of data sources. The Histidine Dihydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Histidine Dihydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Histidine Dihydrochloride, including repackagers and relabelers. The FDA regulates Histidine Dihydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Histidine Dihydrochloride 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 Histidine Dihydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Histidine Dihydrochloride supplier is an individual or a company that provides Histidine Dihydrochloride active pharmaceutical ingredient (API) or Histidine Dihydrochloride finished formulations upon request. The Histidine Dihydrochloride suppliers may include Histidine Dihydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Histidine Dihydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Histidine Dihydrochloride CEP of the European Pharmacopoeia monograph is often referred to as a Histidine Dihydrochloride Certificate of Suitability (COS). The purpose of a Histidine Dihydrochloride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Histidine Dihydrochloride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Histidine Dihydrochloride to their clients by showing that a Histidine Dihydrochloride CEP has been issued for it. The manufacturer submits a Histidine Dihydrochloride CEP (COS) as part of the market authorization procedure, and it takes on the role of a Histidine Dihydrochloride CEP holder for the record. Additionally, the data presented in the Histidine Dihydrochloride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Histidine Dihydrochloride DMF.
A Histidine Dihydrochloride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Histidine Dihydrochloride CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Histidine Dihydrochloride suppliers with CEP (COS) on PharmaCompass.
Histidine Dihydrochloride 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 Histidine Dihydrochloride 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 Histidine Dihydrochloride GMP manufacturer or Histidine Dihydrochloride GMP API supplier for your needs.
A Histidine Dihydrochloride CoA (Certificate of Analysis) is a formal document that attests to Histidine Dihydrochloride's compliance with Histidine Dihydrochloride specifications and serves as a tool for batch-level quality control.
Histidine Dihydrochloride CoA mostly includes findings from lab analyses of a specific batch. For each Histidine Dihydrochloride 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.
Histidine Dihydrochloride may be tested according to a variety of international standards, such as European Pharmacopoeia (Histidine Dihydrochloride EP), Histidine Dihydrochloride JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Histidine Dihydrochloride USP).