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