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ABOUT THIS PAGE
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PharmaCompass offers a list of Carbazochrome 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 Carbazochrome manufacturer or Carbazochrome supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Carbazochrome manufacturer or Carbazochrome supplier.
PharmaCompass also assists you with knowing the Carbazochrome API Price utilized in the formulation of products. Carbazochrome API Price is not always fixed or binding as the Carbazochrome Price is obtained through a variety of data sources. The Carbazochrome Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Adroxon manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Adroxon, including repackagers and relabelers. The FDA regulates Adroxon manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Adroxon 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 Adroxon manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Adroxon supplier is an individual or a company that provides Adroxon active pharmaceutical ingredient (API) or Adroxon finished formulations upon request. The Adroxon suppliers may include Adroxon API manufacturers, exporters, distributors and traders.
click here to find a list of Adroxon suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Adroxon Drug Master File in Japan (Adroxon JDMF) empowers Adroxon API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Adroxon JDMF during the approval evaluation for pharmaceutical products. At the time of Adroxon JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Adroxon suppliers with JDMF on PharmaCompass.
Adroxon 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 Adroxon 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 Adroxon GMP manufacturer or Adroxon GMP API supplier for your needs.
A Adroxon CoA (Certificate of Analysis) is a formal document that attests to Adroxon's compliance with Adroxon specifications and serves as a tool for batch-level quality control.
Adroxon CoA mostly includes findings from lab analyses of a specific batch. For each Adroxon 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.
Adroxon may be tested according to a variety of international standards, such as European Pharmacopoeia (Adroxon EP), Adroxon JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Adroxon USP).
