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