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PharmaCompass offers a list of 4-Amino-3-Phenyl-Butyric 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 4-Amino-3-Phenyl-Butyric Acid manufacturer or 4-Amino-3-Phenyl-Butyric Acid supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred 4-Amino-3-Phenyl-Butyric Acid manufacturer or 4-Amino-3-Phenyl-Butyric Acid supplier.
PharmaCompass also assists you with knowing the 4-Amino-3-Phenyl-Butyric Acid API Price utilized in the formulation of products. 4-Amino-3-Phenyl-Butyric Acid API Price is not always fixed or binding as the 4-Amino-3-Phenyl-Butyric Acid Price is obtained through a variety of data sources. The 4-Amino-3-Phenyl-Butyric Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A AM010359 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AM010359, including repackagers and relabelers. The FDA regulates AM010359 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AM010359 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 AM010359 supplier is an individual or a company that provides AM010359 active pharmaceutical ingredient (API) or AM010359 finished formulations upon request. The AM010359 suppliers may include AM010359 API manufacturers, exporters, distributors and traders.
AM010359 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 AM010359 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 AM010359 GMP manufacturer or AM010359 GMP API supplier for your needs.
A AM010359 CoA (Certificate of Analysis) is a formal document that attests to AM010359's compliance with AM010359 specifications and serves as a tool for batch-level quality control.
AM010359 CoA mostly includes findings from lab analyses of a specific batch. For each AM010359 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.
AM010359 may be tested according to a variety of international standards, such as European Pharmacopoeia (AM010359 EP), AM010359 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (AM010359 USP).