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PharmaCompass offers a list of Metamizole 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 Metamizole manufacturer or Metamizole supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Metamizole manufacturer or Metamizole supplier.
PharmaCompass also assists you with knowing the Metamizole API Price utilized in the formulation of products. Metamizole API Price is not always fixed or binding as the Metamizole Price is obtained through a variety of data sources. The Metamizole Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Metamizole Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Metamizole Sodium, including repackagers and relabelers. The FDA regulates Metamizole Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Metamizole Sodium 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 Metamizole Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Metamizole Sodium supplier is an individual or a company that provides Metamizole Sodium active pharmaceutical ingredient (API) or Metamizole Sodium finished formulations upon request. The Metamizole Sodium suppliers may include Metamizole Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Metamizole Sodium suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Metamizole Sodium DMF (Drug Master File) is a document detailing the whole manufacturing process of Metamizole Sodium active pharmaceutical ingredient (API) in detail. Different forms of Metamizole Sodium DMFs exist exist since differing nations have different regulations, such as Metamizole Sodium USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Metamizole Sodium DMF submitted to regulatory agencies in the US is known as a USDMF. Metamizole Sodium USDMF includes data on Metamizole Sodium's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Metamizole Sodium USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Metamizole Sodium suppliers with USDMF on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Metamizole Sodium Drug Master File in Japan (Metamizole Sodium JDMF) empowers Metamizole Sodium API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Metamizole Sodium JDMF during the approval evaluation for pharmaceutical products. At the time of Metamizole Sodium JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Metamizole Sodium suppliers with JDMF on PharmaCompass.
A Metamizole Sodium CEP of the European Pharmacopoeia monograph is often referred to as a Metamizole Sodium Certificate of Suitability (COS). The purpose of a Metamizole Sodium CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Metamizole Sodium EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Metamizole Sodium to their clients by showing that a Metamizole Sodium CEP has been issued for it. The manufacturer submits a Metamizole Sodium CEP (COS) as part of the market authorization procedure, and it takes on the role of a Metamizole Sodium CEP holder for the record. Additionally, the data presented in the Metamizole Sodium CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Metamizole Sodium DMF.
A Metamizole Sodium CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Metamizole Sodium CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Metamizole Sodium suppliers with CEP (COS) on PharmaCompass.
Metamizole Sodium 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 Metamizole Sodium 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 Metamizole Sodium GMP manufacturer or Metamizole Sodium GMP API supplier for your needs.
A Metamizole Sodium CoA (Certificate of Analysis) is a formal document that attests to Metamizole Sodium's compliance with Metamizole Sodium specifications and serves as a tool for batch-level quality control.
Metamizole Sodium CoA mostly includes findings from lab analyses of a specific batch. For each Metamizole Sodium 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.
Metamizole Sodium may be tested according to a variety of international standards, such as European Pharmacopoeia (Metamizole Sodium EP), Metamizole Sodium JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Metamizole Sodium USP).
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