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