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