Synopsis
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API Suppliers
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USDMF
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CEP/COS
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JDMF
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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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Listed Suppliers
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EDQM
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USP
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JP
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Others
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FDF Dossiers
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FDA Orange Book
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Europe
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Canada
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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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US Exclusivities
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Health Canada Patents
US Medicaid
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Annual Reports
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Regulatory FDF Prices
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API
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FDF
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Data Compilation #PharmaFlow
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Stock Recap #PipelineProspector
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Weekly News Recap #Phispers
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News #PharmaBuzz
ABOUT THIS PAGE
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PharmaCompass offers a list of TAS-117 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 TAS-117 manufacturer or TAS-117 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred TAS-117 manufacturer or TAS-117 supplier.
PharmaCompass also assists you with knowing the TAS-117 API Price utilized in the formulation of products. TAS-117 API Price is not always fixed or binding as the TAS-117 Price is obtained through a variety of data sources. The TAS-117 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A TAS 117 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of TAS 117, including repackagers and relabelers. The FDA regulates TAS 117 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. TAS 117 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A TAS 117 supplier is an individual or a company that provides TAS 117 active pharmaceutical ingredient (API) or TAS 117 finished formulations upon request. The TAS 117 suppliers may include TAS 117 API manufacturers, exporters, distributors and traders.
TAS 117 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 TAS 117 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 TAS 117 GMP manufacturer or TAS 117 GMP API supplier for your needs.
A TAS 117 CoA (Certificate of Analysis) is a formal document that attests to TAS 117's compliance with TAS 117 specifications and serves as a tool for batch-level quality control.
TAS 117 CoA mostly includes findings from lab analyses of a specific batch. For each TAS 117 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.
TAS 117 may be tested according to a variety of international standards, such as European Pharmacopoeia (TAS 117 EP), TAS 117 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (TAS 117 USP).
