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API SUPPLIERS
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ANALYTICAL
ABOUT THIS PAGE
A Fenspiride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fenspiride, including repackagers and relabelers. The FDA regulates Fenspiride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fenspiride 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 Fenspiride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fenspiride supplier is an individual or a company that provides Fenspiride active pharmaceutical ingredient (API) or Fenspiride finished formulations upon request. The Fenspiride suppliers may include Fenspiride API manufacturers, exporters, distributors and traders.
click here to find a list of Fenspiride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Fenspiride written confirmation (Fenspiride WC) is an official document issued by a regulatory agency to a Fenspiride manufacturer, verifying that the manufacturing facility of a Fenspiride active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Fenspiride APIs or Fenspiride finished pharmaceutical products to another nation, regulatory agencies frequently require a Fenspiride WC (written confirmation) as part of the regulatory process.
click here to find a list of Fenspiride suppliers with Written Confirmation (WC) on PharmaCompass.
Fenspiride 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 Fenspiride 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 Fenspiride GMP manufacturer or Fenspiride GMP API supplier for your needs.
A Fenspiride CoA (Certificate of Analysis) is a formal document that attests to Fenspiride's compliance with Fenspiride specifications and serves as a tool for batch-level quality control.
Fenspiride CoA mostly includes findings from lab analyses of a specific batch. For each Fenspiride 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.
Fenspiride may be tested according to a variety of international standards, such as European Pharmacopoeia (Fenspiride EP), Fenspiride JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Fenspiride USP).
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