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PharmaCompass offers a list of Cyclam 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 Cyclam manufacturer or Cyclam supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cyclam manufacturer or Cyclam supplier.
PharmaCompass also assists you with knowing the Cyclam API Price utilized in the formulation of products. Cyclam API Price is not always fixed or binding as the Cyclam Price is obtained through a variety of data sources. The Cyclam Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cyclam manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cyclam, including repackagers and relabelers. The FDA regulates Cyclam manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cyclam API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Cyclam supplier is an individual or a company that provides Cyclam active pharmaceutical ingredient (API) or Cyclam finished formulations upon request. The Cyclam suppliers may include Cyclam API manufacturers, exporters, distributors and traders.
click here to find a list of Cyclam suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cyclam DMF (Drug Master File) is a document detailing the whole manufacturing process of Cyclam active pharmaceutical ingredient (API) in detail. Different forms of Cyclam DMFs exist exist since differing nations have different regulations, such as Cyclam USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Cyclam DMF submitted to regulatory agencies in the US is known as a USDMF. Cyclam USDMF includes data on Cyclam's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Cyclam USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Cyclam suppliers with USDMF on PharmaCompass.
Cyclam 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 Cyclam 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 Cyclam GMP manufacturer or Cyclam GMP API supplier for your needs.
A Cyclam CoA (Certificate of Analysis) is a formal document that attests to Cyclam's compliance with Cyclam specifications and serves as a tool for batch-level quality control.
Cyclam CoA mostly includes findings from lab analyses of a specific batch. For each Cyclam 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.
Cyclam may be tested according to a variety of international standards, such as European Pharmacopoeia (Cyclam EP), Cyclam JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Cyclam USP).