API Suppliers
US DMFs Filed
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JDMFs Filed
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PharmaCompass offers a list of Atorvastatin 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 Atorvastatin manufacturer or Atorvastatin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Atorvastatin manufacturer or Atorvastatin supplier.
PharmaCompass also assists you with knowing the Atorvastatin API Price utilized in the formulation of products. Atorvastatin API Price is not always fixed or binding as the Atorvastatin Price is obtained through a variety of data sources. The Atorvastatin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A MolPort-000-883-773 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-000-883-773, including repackagers and relabelers. The FDA regulates MolPort-000-883-773 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-000-883-773 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A MolPort-000-883-773 supplier is an individual or a company that provides MolPort-000-883-773 active pharmaceutical ingredient (API) or MolPort-000-883-773 finished formulations upon request. The MolPort-000-883-773 suppliers may include MolPort-000-883-773 API manufacturers, exporters, distributors and traders.
click here to find a list of MolPort-000-883-773 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A MolPort-000-883-773 DMF (Drug Master File) is a document detailing the whole manufacturing process of MolPort-000-883-773 active pharmaceutical ingredient (API) in detail. Different forms of MolPort-000-883-773 DMFs exist exist since differing nations have different regulations, such as MolPort-000-883-773 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A MolPort-000-883-773 DMF submitted to regulatory agencies in the US is known as a USDMF. MolPort-000-883-773 USDMF includes data on MolPort-000-883-773's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The MolPort-000-883-773 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 MolPort-000-883-773 Drug Master File in Japan (MolPort-000-883-773 JDMF) empowers MolPort-000-883-773 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 MolPort-000-883-773 JDMF during the approval evaluation for pharmaceutical products. At the time of MolPort-000-883-773 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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In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a MolPort-000-883-773 Drug Master File in Korea (MolPort-000-883-773 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of MolPort-000-883-773. The MFDS reviews the MolPort-000-883-773 KDMF as part of the drug registration process and uses the information provided in the MolPort-000-883-773 KDMF to evaluate the safety and efficacy of the drug.
After submitting a MolPort-000-883-773 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 MolPort-000-883-773 API can apply through the Korea Drug Master File (KDMF).
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A MolPort-000-883-773 CEP of the European Pharmacopoeia monograph is often referred to as a MolPort-000-883-773 Certificate of Suitability (COS). The purpose of a MolPort-000-883-773 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of MolPort-000-883-773 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of MolPort-000-883-773 to their clients by showing that a MolPort-000-883-773 CEP has been issued for it. The manufacturer submits a MolPort-000-883-773 CEP (COS) as part of the market authorization procedure, and it takes on the role of a MolPort-000-883-773 CEP holder for the record. Additionally, the data presented in the MolPort-000-883-773 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the MolPort-000-883-773 DMF.
A MolPort-000-883-773 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. MolPort-000-883-773 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 MolPort-000-883-773 written confirmation (MolPort-000-883-773 WC) is an official document issued by a regulatory agency to a MolPort-000-883-773 manufacturer, verifying that the manufacturing facility of a MolPort-000-883-773 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting MolPort-000-883-773 APIs or MolPort-000-883-773 finished pharmaceutical products to another nation, regulatory agencies frequently require a MolPort-000-883-773 WC (written confirmation) as part of the regulatory process.
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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 MolPort-000-883-773 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for MolPort-000-883-773 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 MolPort-000-883-773 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 MolPort-000-883-773 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a MolPort-000-883-773 NDC to their finished compounded human drug products, they may choose to do so.
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MolPort-000-883-773 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 MolPort-000-883-773 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 MolPort-000-883-773 GMP manufacturer or MolPort-000-883-773 GMP API supplier for your needs.
A MolPort-000-883-773 CoA (Certificate of Analysis) is a formal document that attests to MolPort-000-883-773's compliance with MolPort-000-883-773 specifications and serves as a tool for batch-level quality control.
MolPort-000-883-773 CoA mostly includes findings from lab analyses of a specific batch. For each MolPort-000-883-773 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.
MolPort-000-883-773 may be tested according to a variety of international standards, such as European Pharmacopoeia (MolPort-000-883-773 EP), MolPort-000-883-773 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (MolPort-000-883-773 USP).