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