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ABOUT THIS PAGE
A Ferric Chloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ferric Chloride, including repackagers and relabelers. The FDA regulates Ferric Chloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ferric Chloride 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 Ferric Chloride supplier is an individual or a company that provides Ferric Chloride active pharmaceutical ingredient (API) or Ferric Chloride finished formulations upon request. The Ferric Chloride suppliers may include Ferric Chloride API manufacturers, exporters, distributors and traders.
click here to find a list of Ferric Chloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Ferric Chloride DMF (Drug Master File) is a document detailing the whole manufacturing process of Ferric Chloride active pharmaceutical ingredient (API) in detail. Different forms of Ferric Chloride DMFs exist exist since differing nations have different regulations, such as Ferric Chloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Ferric Chloride DMF submitted to regulatory agencies in the US is known as a USDMF. Ferric Chloride USDMF includes data on Ferric Chloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Ferric Chloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Ferric Chloride suppliers with USDMF on PharmaCompass.
Ferric Chloride 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 Ferric Chloride 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 Ferric Chloride GMP manufacturer or Ferric Chloride GMP API supplier for your needs.
A Ferric Chloride CoA (Certificate of Analysis) is a formal document that attests to Ferric Chloride's compliance with Ferric Chloride specifications and serves as a tool for batch-level quality control.
Ferric Chloride CoA mostly includes findings from lab analyses of a specific batch. For each Ferric Chloride 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.
Ferric Chloride may be tested according to a variety of international standards, such as European Pharmacopoeia (Ferric Chloride EP), Ferric Chloride JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Ferric Chloride USP).
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