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