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