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PharmaCompass offers a list of Sodium Iodide-131 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 Sodium Iodide-131 manufacturer or Sodium Iodide-131 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sodium Iodide-131 manufacturer or Sodium Iodide-131 supplier.
PharmaCompass also assists you with knowing the Sodium Iodide-131 API Price utilized in the formulation of products. Sodium Iodide-131 API Price is not always fixed or binding as the Sodium Iodide-131 Price is obtained through a variety of data sources. The Sodium Iodide-131 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A (131-I)Sodium iodide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of (131-I)Sodium iodide, including repackagers and relabelers. The FDA regulates (131-I)Sodium iodide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. (131-I)Sodium 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 (131-I)Sodium iodide supplier is an individual or a company that provides (131-I)Sodium iodide active pharmaceutical ingredient (API) or (131-I)Sodium iodide finished formulations upon request. The (131-I)Sodium iodide suppliers may include (131-I)Sodium iodide API manufacturers, exporters, distributors and traders.
click here to find a list of (131-I)Sodium iodide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A (131-I)Sodium iodide DMF (Drug Master File) is a document detailing the whole manufacturing process of (131-I)Sodium iodide active pharmaceutical ingredient (API) in detail. Different forms of (131-I)Sodium iodide DMFs exist exist since differing nations have different regulations, such as (131-I)Sodium iodide USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A (131-I)Sodium iodide DMF submitted to regulatory agencies in the US is known as a USDMF. (131-I)Sodium iodide USDMF includes data on (131-I)Sodium iodide's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The (131-I)Sodium iodide USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of (131-I)Sodium iodide suppliers with USDMF on PharmaCompass.
(131-I)Sodium 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 (131-I)Sodium 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 (131-I)Sodium iodide GMP manufacturer or (131-I)Sodium iodide GMP API supplier for your needs.
A (131-I)Sodium iodide CoA (Certificate of Analysis) is a formal document that attests to (131-I)Sodium iodide's compliance with (131-I)Sodium iodide specifications and serves as a tool for batch-level quality control.
(131-I)Sodium iodide CoA mostly includes findings from lab analyses of a specific batch. For each (131-I)Sodium 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.
(131-I)Sodium iodide may be tested according to a variety of international standards, such as European Pharmacopoeia ((131-I)Sodium iodide EP), (131-I)Sodium iodide JP (Japanese Pharmacopeia) and the US Pharmacopoeia ((131-I)Sodium iodide USP).