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PharmaCompass offers a list of GB0139 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 GB0139 manufacturer or GB0139 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred GB0139 manufacturer or GB0139 supplier.
PharmaCompass also assists you with knowing the GB0139 API Price utilized in the formulation of products. GB0139 API Price is not always fixed or binding as the GB0139 Price is obtained through a variety of data sources. The GB0139 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A TD 139 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of TD 139, including repackagers and relabelers. The FDA regulates TD 139 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. TD 139 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 TD 139 supplier is an individual or a company that provides TD 139 active pharmaceutical ingredient (API) or TD 139 finished formulations upon request. The TD 139 suppliers may include TD 139 API manufacturers, exporters, distributors and traders.
TD 139 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 TD 139 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 TD 139 GMP manufacturer or TD 139 GMP API supplier for your needs.
A TD 139 CoA (Certificate of Analysis) is a formal document that attests to TD 139's compliance with TD 139 specifications and serves as a tool for batch-level quality control.
TD 139 CoA mostly includes findings from lab analyses of a specific batch. For each TD 139 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.
TD 139 may be tested according to a variety of international standards, such as European Pharmacopoeia (TD 139 EP), TD 139 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (TD 139 USP).