Synopsis
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USDMF
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CEP/COS
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EU WC
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KDMF
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NDC API
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VMF
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API
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FDF
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Europe
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Australia
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South Africa
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Listed Dossiers
DRUG PRODUCT COMPOSITIONS
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US Patents
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Data Compilation #PharmaFlow
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Stock Recap #PipelineProspector
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Weekly News Recap #Phispers
US Medicaid
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Annual Reports
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Finished Drug Prices
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API SUPPLIERS
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]
Listed Suppliers
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]FDF Dossiers
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Related Excipient Companies
Rochem International Inc
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]SPI Pharma
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Pharm-RX Chemical
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Nanjing Well Pharmaceutical
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Pfanstiehl
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Actylis
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]BioSpectra
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Finar
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Gangwal Chemicals
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Kerry
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Topical
Thickeners and Stabilizers
Parenteral
Co-Processed Excipients
Coating Systems & Additives
Solubilizers
Controlled & Modified Release
Film Formers & Plasticizers
Rheology Modifiers
Taste Masking
Direct Compression
Emulsifying Agents
API Stability Enhancers
Digital Content
NEWS #PharmaBuzz
REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
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).
