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