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