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PharmaCompass offers a list of AC-424 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 AC-424 manufacturer or AC-424 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred AC-424 manufacturer or AC-424 supplier.
PharmaCompass also assists you with knowing the AC-424 API Price utilized in the formulation of products. AC-424 API Price is not always fixed or binding as the AC-424 Price is obtained through a variety of data sources. The AC-424 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Febantelum manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Febantelum, including repackagers and relabelers. The FDA regulates Febantelum manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Febantelum 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 Febantelum manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Febantelum supplier is an individual or a company that provides Febantelum active pharmaceutical ingredient (API) or Febantelum finished formulations upon request. The Febantelum suppliers may include Febantelum API manufacturers, exporters, distributors and traders.
click here to find a list of Febantelum suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Febantelum CEP of the European Pharmacopoeia monograph is often referred to as a Febantelum Certificate of Suitability (COS). The purpose of a Febantelum CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Febantelum EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Febantelum to their clients by showing that a Febantelum CEP has been issued for it. The manufacturer submits a Febantelum CEP (COS) as part of the market authorization procedure, and it takes on the role of a Febantelum CEP holder for the record. Additionally, the data presented in the Febantelum CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Febantelum DMF.
A Febantelum CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Febantelum 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 Febantelum suppliers with CEP (COS) on PharmaCompass.
Febantelum 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 Febantelum 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 Febantelum GMP manufacturer or Febantelum GMP API supplier for your needs.
A Febantelum CoA (Certificate of Analysis) is a formal document that attests to Febantelum's compliance with Febantelum specifications and serves as a tool for batch-level quality control.
Febantelum CoA mostly includes findings from lab analyses of a specific batch. For each Febantelum 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.
Febantelum may be tested according to a variety of international standards, such as European Pharmacopoeia (Febantelum EP), Febantelum JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Febantelum USP).
