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