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