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