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