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ABOUT THIS PAGE
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PharmaCompass offers a list of Phenethylamine 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 Phenethylamine manufacturer or Phenethylamine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Phenethylamine manufacturer or Phenethylamine supplier.
PharmaCompass also assists you with knowing the Phenethylamine API Price utilized in the formulation of products. Phenethylamine API Price is not always fixed or binding as the Phenethylamine Price is obtained through a variety of data sources. The Phenethylamine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A beta-phenylethylamine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of beta-phenylethylamine, including repackagers and relabelers. The FDA regulates beta-phenylethylamine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. beta-phenylethylamine 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 beta-phenylethylamine supplier is an individual or a company that provides beta-phenylethylamine active pharmaceutical ingredient (API) or beta-phenylethylamine finished formulations upon request. The beta-phenylethylamine suppliers may include beta-phenylethylamine API manufacturers, exporters, distributors and traders.
click here to find a list of beta-phenylethylamine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A beta-phenylethylamine DMF (Drug Master File) is a document detailing the whole manufacturing process of beta-phenylethylamine active pharmaceutical ingredient (API) in detail. Different forms of beta-phenylethylamine DMFs exist exist since differing nations have different regulations, such as beta-phenylethylamine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A beta-phenylethylamine DMF submitted to regulatory agencies in the US is known as a USDMF. beta-phenylethylamine USDMF includes data on beta-phenylethylamine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The beta-phenylethylamine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of beta-phenylethylamine suppliers with USDMF on PharmaCompass.
beta-phenylethylamine 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 beta-phenylethylamine 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 beta-phenylethylamine GMP manufacturer or beta-phenylethylamine GMP API supplier for your needs.
A beta-phenylethylamine CoA (Certificate of Analysis) is a formal document that attests to beta-phenylethylamine's compliance with beta-phenylethylamine specifications and serves as a tool for batch-level quality control.
beta-phenylethylamine CoA mostly includes findings from lab analyses of a specific batch. For each beta-phenylethylamine 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.
beta-phenylethylamine may be tested according to a variety of international standards, such as European Pharmacopoeia (beta-phenylethylamine EP), beta-phenylethylamine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (beta-phenylethylamine USP).
