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