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