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