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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 PREVACARE R manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of PREVACARE R, including repackagers and relabelers. The FDA regulates PREVACARE R manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. PREVACARE R 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 PREVACARE R manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A PREVACARE R supplier is an individual or a company that provides PREVACARE R active pharmaceutical ingredient (API) or PREVACARE R finished formulations upon request. The PREVACARE R suppliers may include PREVACARE R API manufacturers, exporters, distributors and traders.
click here to find a list of PREVACARE R suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A PREVACARE R DMF (Drug Master File) is a document detailing the whole manufacturing process of PREVACARE R active pharmaceutical ingredient (API) in detail. Different forms of PREVACARE R DMFs exist exist since differing nations have different regulations, such as PREVACARE R USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A PREVACARE R DMF submitted to regulatory agencies in the US is known as a USDMF. PREVACARE R USDMF includes data on PREVACARE R's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The PREVACARE R USDMF is kept confidential to protect the manufacturer’s intellectual property.
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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 PREVACARE R Drug Master File in Japan (PREVACARE R JDMF) empowers PREVACARE R 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 PREVACARE R JDMF during the approval evaluation for pharmaceutical products. At the time of PREVACARE R JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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A PREVACARE R CEP of the European Pharmacopoeia monograph is often referred to as a PREVACARE R Certificate of Suitability (COS). The purpose of a PREVACARE R CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of PREVACARE R EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of PREVACARE R to their clients by showing that a PREVACARE R CEP has been issued for it. The manufacturer submits a PREVACARE R CEP (COS) as part of the market authorization procedure, and it takes on the role of a PREVACARE R CEP holder for the record. Additionally, the data presented in the PREVACARE R CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the PREVACARE R DMF.
A PREVACARE R CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. PREVACARE R CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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A PREVACARE R written confirmation (PREVACARE R WC) is an official document issued by a regulatory agency to a PREVACARE R manufacturer, verifying that the manufacturing facility of a PREVACARE R active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting PREVACARE R APIs or PREVACARE R finished pharmaceutical products to another nation, regulatory agencies frequently require a PREVACARE R WC (written confirmation) as part of the regulatory process.
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PREVACARE R 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 PREVACARE R 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 PREVACARE R GMP manufacturer or PREVACARE R GMP API supplier for your needs.
A PREVACARE R CoA (Certificate of Analysis) is a formal document that attests to PREVACARE R's compliance with PREVACARE R specifications and serves as a tool for batch-level quality control.
PREVACARE R CoA mostly includes findings from lab analyses of a specific batch. For each PREVACARE R 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.
PREVACARE R may be tested according to a variety of international standards, such as European Pharmacopoeia (PREVACARE R EP), PREVACARE R JP (Japanese Pharmacopeia) and the US Pharmacopoeia (PREVACARE R USP).