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