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