API Suppliers
US DMFs Filed
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CEP/COS Certifications
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JDMFs Filed
Other Certificates
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Other Suppliers
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USA (Orange Book)
Europe
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Australia
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South Africa
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U.S. Medicaid
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PharmaCompass offers a list of Tannins 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 Tannins manufacturer or Tannins supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tannins manufacturer or Tannins supplier.
PharmaCompass also assists you with knowing the Tannins API Price utilized in the formulation of products. Tannins API Price is not always fixed or binding as the Tannins Price is obtained through a variety of data sources. The Tannins Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tannins manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tannins, including repackagers and relabelers. The FDA regulates Tannins manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tannins 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 Tannins manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tannins supplier is an individual or a company that provides Tannins active pharmaceutical ingredient (API) or Tannins finished formulations upon request. The Tannins suppliers may include Tannins API manufacturers, exporters, distributors and traders.
click here to find a list of Tannins suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information 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 Tannins Drug Master File in Japan (Tannins JDMF) empowers Tannins 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 Tannins JDMF during the approval evaluation for pharmaceutical products. At the time of Tannins 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 Tannins suppliers with JDMF on PharmaCompass.
Tannins 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 Tannins 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 Tannins GMP manufacturer or Tannins GMP API supplier for your needs.
A Tannins CoA (Certificate of Analysis) is a formal document that attests to Tannins's compliance with Tannins specifications and serves as a tool for batch-level quality control.
Tannins CoA mostly includes findings from lab analyses of a specific batch. For each Tannins 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.
Tannins may be tested according to a variety of international standards, such as European Pharmacopoeia (Tannins EP), Tannins JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Tannins USP).