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PharmaCompass offers a list of Deferiprone 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 Deferiprone manufacturer or Deferiprone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Deferiprone manufacturer or Deferiprone supplier.
PharmaCompass also assists you with knowing the Deferiprone API Price utilized in the formulation of products. Deferiprone API Price is not always fixed or binding as the Deferiprone Price is obtained through a variety of data sources. The Deferiprone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ferriprox manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ferriprox, including repackagers and relabelers. The FDA regulates Ferriprox manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ferriprox 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 Ferriprox manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ferriprox supplier is an individual or a company that provides Ferriprox active pharmaceutical ingredient (API) or Ferriprox finished formulations upon request. The Ferriprox suppliers may include Ferriprox API manufacturers, exporters, distributors and traders.
click here to find a list of Ferriprox suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Ferriprox DMF (Drug Master File) is a document detailing the whole manufacturing process of Ferriprox active pharmaceutical ingredient (API) in detail. Different forms of Ferriprox DMFs exist exist since differing nations have different regulations, such as Ferriprox USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Ferriprox DMF submitted to regulatory agencies in the US is known as a USDMF. Ferriprox USDMF includes data on Ferriprox's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Ferriprox USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Ferriprox suppliers with USDMF on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Ferriprox Drug Master File in Korea (Ferriprox KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Ferriprox. The MFDS reviews the Ferriprox KDMF as part of the drug registration process and uses the information provided in the Ferriprox KDMF to evaluate the safety and efficacy of the drug.
After submitting a Ferriprox KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Ferriprox API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Ferriprox suppliers with KDMF on PharmaCompass.
A Ferriprox CEP of the European Pharmacopoeia monograph is often referred to as a Ferriprox Certificate of Suitability (COS). The purpose of a Ferriprox CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Ferriprox EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Ferriprox to their clients by showing that a Ferriprox CEP has been issued for it. The manufacturer submits a Ferriprox CEP (COS) as part of the market authorization procedure, and it takes on the role of a Ferriprox CEP holder for the record. Additionally, the data presented in the Ferriprox CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Ferriprox DMF.
A Ferriprox CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Ferriprox 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 Ferriprox suppliers with CEP (COS) on PharmaCompass.
A Ferriprox written confirmation (Ferriprox WC) is an official document issued by a regulatory agency to a Ferriprox manufacturer, verifying that the manufacturing facility of a Ferriprox active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Ferriprox APIs or Ferriprox finished pharmaceutical products to another nation, regulatory agencies frequently require a Ferriprox WC (written confirmation) as part of the regulatory process.
click here to find a list of Ferriprox suppliers with Written Confirmation (WC) on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Ferriprox as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Ferriprox API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Ferriprox as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Ferriprox and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Ferriprox NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Ferriprox suppliers with NDC on PharmaCompass.
Ferriprox 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 Ferriprox 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 Ferriprox GMP manufacturer or Ferriprox GMP API supplier for your needs.
A Ferriprox CoA (Certificate of Analysis) is a formal document that attests to Ferriprox's compliance with Ferriprox specifications and serves as a tool for batch-level quality control.
Ferriprox CoA mostly includes findings from lab analyses of a specific batch. For each Ferriprox 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.
Ferriprox may be tested according to a variety of international standards, such as European Pharmacopoeia (Ferriprox EP), Ferriprox JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Ferriprox USP).
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