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PharmaCompass offers a list of Ribavirin 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 Ribavirin manufacturer or Ribavirin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ribavirin manufacturer or Ribavirin supplier.
PharmaCompass also assists you with knowing the Ribavirin API Price utilized in the formulation of products. Ribavirin API Price is not always fixed or binding as the Ribavirin Price is obtained through a variety of data sources. The Ribavirin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ribavirin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ribavirin, including repackagers and relabelers. The FDA regulates Ribavirin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ribavirin 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 Ribavirin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ribavirin supplier is an individual or a company that provides Ribavirin active pharmaceutical ingredient (API) or Ribavirin finished formulations upon request. The Ribavirin suppliers may include Ribavirin API manufacturers, exporters, distributors and traders.
click here to find a list of Ribavirin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Ribavirin DMF (Drug Master File) is a document detailing the whole manufacturing process of Ribavirin active pharmaceutical ingredient (API) in detail. Different forms of Ribavirin DMFs exist exist since differing nations have different regulations, such as Ribavirin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Ribavirin DMF submitted to regulatory agencies in the US is known as a USDMF. Ribavirin USDMF includes data on Ribavirin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Ribavirin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Ribavirin 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 Ribavirin Drug Master File in Japan (Ribavirin JDMF) empowers Ribavirin 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 Ribavirin JDMF during the approval evaluation for pharmaceutical products. At the time of Ribavirin 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 Ribavirin suppliers with JDMF on PharmaCompass.
A Ribavirin CEP of the European Pharmacopoeia monograph is often referred to as a Ribavirin Certificate of Suitability (COS). The purpose of a Ribavirin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Ribavirin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Ribavirin to their clients by showing that a Ribavirin CEP has been issued for it. The manufacturer submits a Ribavirin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Ribavirin CEP holder for the record. Additionally, the data presented in the Ribavirin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Ribavirin DMF.
A Ribavirin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Ribavirin 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 Ribavirin suppliers with CEP (COS) on PharmaCompass.
A Ribavirin written confirmation (Ribavirin WC) is an official document issued by a regulatory agency to a Ribavirin manufacturer, verifying that the manufacturing facility of a Ribavirin active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Ribavirin APIs or Ribavirin finished pharmaceutical products to another nation, regulatory agencies frequently require a Ribavirin WC (written confirmation) as part of the regulatory process.
click here to find a list of Ribavirin 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 Ribavirin as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Ribavirin 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 Ribavirin 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 Ribavirin and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Ribavirin NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Ribavirin suppliers with NDC on PharmaCompass.
Ribavirin 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 Ribavirin 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 Ribavirin GMP manufacturer or Ribavirin GMP API supplier for your needs.
A Ribavirin CoA (Certificate of Analysis) is a formal document that attests to Ribavirin's compliance with Ribavirin specifications and serves as a tool for batch-level quality control.
Ribavirin CoA mostly includes findings from lab analyses of a specific batch. For each Ribavirin 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.
Ribavirin may be tested according to a variety of international standards, such as European Pharmacopoeia (Ribavirin EP), Ribavirin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Ribavirin USP).