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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 GB0139 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of GB0139, including repackagers and relabelers. The FDA regulates GB0139 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. GB0139 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 GB0139 supplier is an individual or a company that provides GB0139 active pharmaceutical ingredient (API) or GB0139 finished formulations upon request. The GB0139 suppliers may include GB0139 API manufacturers, exporters, distributors and traders.
GB0139 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 GB0139 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 GB0139 GMP manufacturer or GB0139 GMP API supplier for your needs.
A GB0139 CoA (Certificate of Analysis) is a formal document that attests to GB0139's compliance with GB0139 specifications and serves as a tool for batch-level quality control.
GB0139 CoA mostly includes findings from lab analyses of a specific batch. For each GB0139 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.
GB0139 may be tested according to a variety of international standards, such as European Pharmacopoeia (GB0139 EP), GB0139 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (GB0139 USP).
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