X
API Suppliers
US DMFs Filed
0
CEP/COS Certifications
JDMFs Filed
Other Certificates
0
Other Suppliers
USA (Orange Book)
0
Europe
Canada
Australia
0
South Africa
Uploaded Dossiers
U.S. Medicaid
0
Annual Reports
0
0
52
PharmaCompass offers a list of Dequalinium Chloride 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 Dequalinium Chloride manufacturer or Dequalinium Chloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dequalinium Chloride manufacturer or Dequalinium Chloride supplier.
PharmaCompass also assists you with knowing the Dequalinium Chloride API Price utilized in the formulation of products. Dequalinium Chloride API Price is not always fixed or binding as the Dequalinium Chloride Price is obtained through a variety of data sources. The Dequalinium Chloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 1,10-Decamethylene-bis(4-aminoquinaldinium chloride) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 1,10-Decamethylene-bis(4-aminoquinaldinium chloride), including repackagers and relabelers. The FDA regulates 1,10-Decamethylene-bis(4-aminoquinaldinium chloride) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 1,10-Decamethylene-bis(4-aminoquinaldinium chloride) 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 1,10-Decamethylene-bis(4-aminoquinaldinium chloride) manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 1,10-Decamethylene-bis(4-aminoquinaldinium chloride) supplier is an individual or a company that provides 1,10-Decamethylene-bis(4-aminoquinaldinium chloride) active pharmaceutical ingredient (API) or 1,10-Decamethylene-bis(4-aminoquinaldinium chloride) finished formulations upon request. The 1,10-Decamethylene-bis(4-aminoquinaldinium chloride) suppliers may include 1,10-Decamethylene-bis(4-aminoquinaldinium chloride) API manufacturers, exporters, distributors and traders.
click here to find a list of 1,10-Decamethylene-bis(4-aminoquinaldinium chloride) 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 1,10-Decamethylene-bis(4-aminoquinaldinium chloride) Drug Master File in Japan (1,10-Decamethylene-bis(4-aminoquinaldinium chloride) JDMF) empowers 1,10-Decamethylene-bis(4-aminoquinaldinium chloride) 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 1,10-Decamethylene-bis(4-aminoquinaldinium chloride) JDMF during the approval evaluation for pharmaceutical products. At the time of 1,10-Decamethylene-bis(4-aminoquinaldinium chloride) 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 1,10-Decamethylene-bis(4-aminoquinaldinium chloride) suppliers with JDMF on PharmaCompass.
A 1,10-Decamethylene-bis(4-aminoquinaldinium chloride) CEP of the European Pharmacopoeia monograph is often referred to as a 1,10-Decamethylene-bis(4-aminoquinaldinium chloride) Certificate of Suitability (COS). The purpose of a 1,10-Decamethylene-bis(4-aminoquinaldinium chloride) CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of 1,10-Decamethylene-bis(4-aminoquinaldinium chloride) EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of 1,10-Decamethylene-bis(4-aminoquinaldinium chloride) to their clients by showing that a 1,10-Decamethylene-bis(4-aminoquinaldinium chloride) CEP has been issued for it. The manufacturer submits a 1,10-Decamethylene-bis(4-aminoquinaldinium chloride) CEP (COS) as part of the market authorization procedure, and it takes on the role of a 1,10-Decamethylene-bis(4-aminoquinaldinium chloride) CEP holder for the record. Additionally, the data presented in the 1,10-Decamethylene-bis(4-aminoquinaldinium chloride) CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the 1,10-Decamethylene-bis(4-aminoquinaldinium chloride) DMF.
A 1,10-Decamethylene-bis(4-aminoquinaldinium chloride) CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. 1,10-Decamethylene-bis(4-aminoquinaldinium chloride) CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of 1,10-Decamethylene-bis(4-aminoquinaldinium chloride) suppliers with CEP (COS) on PharmaCompass.
1,10-Decamethylene-bis(4-aminoquinaldinium chloride) 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 1,10-Decamethylene-bis(4-aminoquinaldinium chloride) 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 1,10-Decamethylene-bis(4-aminoquinaldinium chloride) GMP manufacturer or 1,10-Decamethylene-bis(4-aminoquinaldinium chloride) GMP API supplier for your needs.
A 1,10-Decamethylene-bis(4-aminoquinaldinium chloride) CoA (Certificate of Analysis) is a formal document that attests to 1,10-Decamethylene-bis(4-aminoquinaldinium chloride)'s compliance with 1,10-Decamethylene-bis(4-aminoquinaldinium chloride) specifications and serves as a tool for batch-level quality control.
1,10-Decamethylene-bis(4-aminoquinaldinium chloride) CoA mostly includes findings from lab analyses of a specific batch. For each 1,10-Decamethylene-bis(4-aminoquinaldinium chloride) 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.
1,10-Decamethylene-bis(4-aminoquinaldinium chloride) may be tested according to a variety of international standards, such as European Pharmacopoeia (1,10-Decamethylene-bis(4-aminoquinaldinium chloride) EP), 1,10-Decamethylene-bis(4-aminoquinaldinium chloride) JP (Japanese Pharmacopeia) and the US Pharmacopoeia (1,10-Decamethylene-bis(4-aminoquinaldinium chloride) USP).
Market Place
