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PharmaCompass offers a list of P-Coumaric Acid 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 P-Coumaric Acid manufacturer or P-Coumaric Acid supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred P-Coumaric Acid manufacturer or P-Coumaric Acid supplier.
PharmaCompass also assists you with knowing the P-Coumaric Acid API Price utilized in the formulation of products. P-Coumaric Acid API Price is not always fixed or binding as the P-Coumaric Acid Price is obtained through a variety of data sources. The P-Coumaric Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A AM20050138 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AM20050138, including repackagers and relabelers. The FDA regulates AM20050138 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AM20050138 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 AM20050138 supplier is an individual or a company that provides AM20050138 active pharmaceutical ingredient (API) or AM20050138 finished formulations upon request. The AM20050138 suppliers may include AM20050138 API manufacturers, exporters, distributors and traders.
AM20050138 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 AM20050138 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 AM20050138 GMP manufacturer or AM20050138 GMP API supplier for your needs.
A AM20050138 CoA (Certificate of Analysis) is a formal document that attests to AM20050138's compliance with AM20050138 specifications and serves as a tool for batch-level quality control.
AM20050138 CoA mostly includes findings from lab analyses of a specific batch. For each AM20050138 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.
AM20050138 may be tested according to a variety of international standards, such as European Pharmacopoeia (AM20050138 EP), AM20050138 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (AM20050138 USP).
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