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