API Suppliers
US DMFs Filed
CEP/COS Certifications
JDMFs Filed
Other Certificates
Other Suppliers
0
USA (Orange Book)
Europe
Canada
Australia
0
South Africa
Uploaded Dossiers
U.S. Medicaid
Annual Reports
0
53
PharmaCompass offers a list of Chlorhexidine Gluconate 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 Chlorhexidine Gluconate manufacturer or Chlorhexidine Gluconate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Chlorhexidine Gluconate manufacturer or Chlorhexidine Gluconate supplier.
PharmaCompass also assists you with knowing the Chlorhexidine Gluconate API Price utilized in the formulation of products. Chlorhexidine Gluconate API Price is not always fixed or binding as the Chlorhexidine Gluconate Price is obtained through a variety of data sources. The Chlorhexidine Gluconate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Chlorhexidine Gluconate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Chlorhexidine Gluconate, including repackagers and relabelers. The FDA regulates Chlorhexidine Gluconate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Chlorhexidine Gluconate 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 Chlorhexidine Gluconate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Chlorhexidine Gluconate supplier is an individual or a company that provides Chlorhexidine Gluconate active pharmaceutical ingredient (API) or Chlorhexidine Gluconate finished formulations upon request. The Chlorhexidine Gluconate suppliers may include Chlorhexidine Gluconate API manufacturers, exporters, distributors and traders.
click here to find a list of Chlorhexidine Gluconate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Chlorhexidine Gluconate DMF (Drug Master File) is a document detailing the whole manufacturing process of Chlorhexidine Gluconate active pharmaceutical ingredient (API) in detail. Different forms of Chlorhexidine Gluconate DMFs exist exist since differing nations have different regulations, such as Chlorhexidine Gluconate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Chlorhexidine Gluconate DMF submitted to regulatory agencies in the US is known as a USDMF. Chlorhexidine Gluconate USDMF includes data on Chlorhexidine Gluconate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Chlorhexidine Gluconate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Chlorhexidine Gluconate suppliers with USDMF 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 Chlorhexidine Gluconate Drug Master File in Japan (Chlorhexidine Gluconate JDMF) empowers Chlorhexidine Gluconate 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 Chlorhexidine Gluconate JDMF during the approval evaluation for pharmaceutical products. At the time of Chlorhexidine Gluconate 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 Chlorhexidine Gluconate suppliers with JDMF on PharmaCompass.
A Chlorhexidine Gluconate CEP of the European Pharmacopoeia monograph is often referred to as a Chlorhexidine Gluconate Certificate of Suitability (COS). The purpose of a Chlorhexidine Gluconate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Chlorhexidine Gluconate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Chlorhexidine Gluconate to their clients by showing that a Chlorhexidine Gluconate CEP has been issued for it. The manufacturer submits a Chlorhexidine Gluconate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Chlorhexidine Gluconate CEP holder for the record. Additionally, the data presented in the Chlorhexidine Gluconate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Chlorhexidine Gluconate DMF.
A Chlorhexidine Gluconate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Chlorhexidine Gluconate 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 Chlorhexidine Gluconate suppliers with CEP (COS) on PharmaCompass.
A Chlorhexidine Gluconate written confirmation (Chlorhexidine Gluconate WC) is an official document issued by a regulatory agency to a Chlorhexidine Gluconate manufacturer, verifying that the manufacturing facility of a Chlorhexidine Gluconate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Chlorhexidine Gluconate APIs or Chlorhexidine Gluconate finished pharmaceutical products to another nation, regulatory agencies frequently require a Chlorhexidine Gluconate WC (written confirmation) as part of the regulatory process.
click here to find a list of Chlorhexidine Gluconate suppliers with Written Confirmation (WC) on PharmaCompass.
Chlorhexidine Gluconate 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 Chlorhexidine Gluconate 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 Chlorhexidine Gluconate GMP manufacturer or Chlorhexidine Gluconate GMP API supplier for your needs.
A Chlorhexidine Gluconate CoA (Certificate of Analysis) is a formal document that attests to Chlorhexidine Gluconate's compliance with Chlorhexidine Gluconate specifications and serves as a tool for batch-level quality control.
Chlorhexidine Gluconate CoA mostly includes findings from lab analyses of a specific batch. For each Chlorhexidine Gluconate 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.
Chlorhexidine Gluconate may be tested according to a variety of international standards, such as European Pharmacopoeia (Chlorhexidine Gluconate EP), Chlorhexidine Gluconate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Chlorhexidine Gluconate USP).