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API SUPPLIERS
Jai Radhe Sales is your partner for all your sourcing needs.
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Jai Radhe Sales is your partner for all your sourcing needs.
About the Company : Jai Radhe Sales was founded in 1999 as an out-of-the-box distribution firm specializing in the global supply of high-quality pharmaceutical ingredients. The firm provides complete ...
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PharmaCompass offers a list of Carprofen 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 Carprofen manufacturer or Carprofen supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Carprofen manufacturer or Carprofen supplier.
PharmaCompass also assists you with knowing the Carprofen API Price utilized in the formulation of products. Carprofen API Price is not always fixed or binding as the Carprofen Price is obtained through a variety of data sources. The Carprofen Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Carprodyl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Carprodyl, including repackagers and relabelers. The FDA regulates Carprodyl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Carprodyl 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 Carprodyl manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Carprodyl supplier is an individual or a company that provides Carprodyl active pharmaceutical ingredient (API) or Carprodyl finished formulations upon request. The Carprodyl suppliers may include Carprodyl API manufacturers, exporters, distributors and traders.
click here to find a list of Carprodyl suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Carprodyl DMF (Drug Master File) is a document detailing the whole manufacturing process of Carprodyl active pharmaceutical ingredient (API) in detail. Different forms of Carprodyl DMFs exist exist since differing nations have different regulations, such as Carprodyl USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Carprodyl DMF submitted to regulatory agencies in the US is known as a USDMF. Carprodyl USDMF includes data on Carprodyl's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Carprodyl USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Carprodyl suppliers with USDMF on PharmaCompass.
A Carprodyl CEP of the European Pharmacopoeia monograph is often referred to as a Carprodyl Certificate of Suitability (COS). The purpose of a Carprodyl CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Carprodyl EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Carprodyl to their clients by showing that a Carprodyl CEP has been issued for it. The manufacturer submits a Carprodyl CEP (COS) as part of the market authorization procedure, and it takes on the role of a Carprodyl CEP holder for the record. Additionally, the data presented in the Carprodyl CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Carprodyl DMF.
A Carprodyl CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Carprodyl 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 Carprodyl suppliers with CEP (COS) on PharmaCompass.
A Carprodyl written confirmation (Carprodyl WC) is an official document issued by a regulatory agency to a Carprodyl manufacturer, verifying that the manufacturing facility of a Carprodyl active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Carprodyl APIs or Carprodyl finished pharmaceutical products to another nation, regulatory agencies frequently require a Carprodyl WC (written confirmation) as part of the regulatory process.
click here to find a list of Carprodyl 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 Carprodyl as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Carprodyl 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 Carprodyl 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 Carprodyl and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Carprodyl NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Carprodyl suppliers with NDC on PharmaCompass.
Carprodyl 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 Carprodyl 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 Carprodyl GMP manufacturer or Carprodyl GMP API supplier for your needs.
A Carprodyl CoA (Certificate of Analysis) is a formal document that attests to Carprodyl's compliance with Carprodyl specifications and serves as a tool for batch-level quality control.
Carprodyl CoA mostly includes findings from lab analyses of a specific batch. For each Carprodyl 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.
Carprodyl may be tested according to a variety of international standards, such as European Pharmacopoeia (Carprodyl EP), Carprodyl JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Carprodyl USP).
