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PharmaCompass offers a list of Enoxaparin Sodium 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 Enoxaparin Sodium manufacturer or Enoxaparin Sodium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Enoxaparin Sodium manufacturer or Enoxaparin Sodium supplier.
PharmaCompass also assists you with knowing the Enoxaparin Sodium API Price utilized in the formulation of products. Enoxaparin Sodium API Price is not always fixed or binding as the Enoxaparin Sodium Price is obtained through a variety of data sources. The Enoxaparin Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Enoxaparin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Enoxaparin, including repackagers and relabelers. The FDA regulates Enoxaparin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Enoxaparin 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 Enoxaparin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Enoxaparin supplier is an individual or a company that provides Enoxaparin active pharmaceutical ingredient (API) or Enoxaparin finished formulations upon request. The Enoxaparin suppliers may include Enoxaparin API manufacturers, exporters, distributors and traders.
click here to find a list of Enoxaparin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Enoxaparin DMF (Drug Master File) is a document detailing the whole manufacturing process of Enoxaparin active pharmaceutical ingredient (API) in detail. Different forms of Enoxaparin DMFs exist exist since differing nations have different regulations, such as Enoxaparin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Enoxaparin DMF submitted to regulatory agencies in the US is known as a USDMF. Enoxaparin USDMF includes data on Enoxaparin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Enoxaparin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Enoxaparin suppliers with USDMF on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Enoxaparin Drug Master File in Korea (Enoxaparin KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Enoxaparin. The MFDS reviews the Enoxaparin KDMF as part of the drug registration process and uses the information provided in the Enoxaparin KDMF to evaluate the safety and efficacy of the drug.
After submitting a Enoxaparin KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Enoxaparin API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Enoxaparin suppliers with KDMF on PharmaCompass.
A Enoxaparin CEP of the European Pharmacopoeia monograph is often referred to as a Enoxaparin Certificate of Suitability (COS). The purpose of a Enoxaparin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Enoxaparin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Enoxaparin to their clients by showing that a Enoxaparin CEP has been issued for it. The manufacturer submits a Enoxaparin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Enoxaparin CEP holder for the record. Additionally, the data presented in the Enoxaparin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Enoxaparin DMF.
A Enoxaparin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Enoxaparin 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 Enoxaparin suppliers with CEP (COS) on PharmaCompass.
A Enoxaparin written confirmation (Enoxaparin WC) is an official document issued by a regulatory agency to a Enoxaparin manufacturer, verifying that the manufacturing facility of a Enoxaparin active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Enoxaparin APIs or Enoxaparin finished pharmaceutical products to another nation, regulatory agencies frequently require a Enoxaparin WC (written confirmation) as part of the regulatory process.
click here to find a list of Enoxaparin suppliers with Written Confirmation (WC) on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Enoxaparin as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Enoxaparin API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Enoxaparin as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Enoxaparin and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Enoxaparin NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Enoxaparin suppliers with NDC on PharmaCompass.
Enoxaparin 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 Enoxaparin 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 Enoxaparin GMP manufacturer or Enoxaparin GMP API supplier for your needs.
A Enoxaparin CoA (Certificate of Analysis) is a formal document that attests to Enoxaparin's compliance with Enoxaparin specifications and serves as a tool for batch-level quality control.
Enoxaparin CoA mostly includes findings from lab analyses of a specific batch. For each Enoxaparin 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.
Enoxaparin may be tested according to a variety of international standards, such as European Pharmacopoeia (Enoxaparin EP), Enoxaparin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Enoxaparin USP).