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API SUPPLIERS
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Faran Shimi Pharmaceutical
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REF. STANDARDS & IMPURITIES
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ANALYTICAL
ABOUT THIS PAGE
A Flurbiprofen Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Flurbiprofen Sodium, including repackagers and relabelers. The FDA regulates Flurbiprofen Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Flurbiprofen Sodium 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 Flurbiprofen Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Flurbiprofen Sodium supplier is an individual or a company that provides Flurbiprofen Sodium active pharmaceutical ingredient (API) or Flurbiprofen Sodium finished formulations upon request. The Flurbiprofen Sodium suppliers may include Flurbiprofen Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Flurbiprofen Sodium suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Flurbiprofen Sodium DMF (Drug Master File) is a document detailing the whole manufacturing process of Flurbiprofen Sodium active pharmaceutical ingredient (API) in detail. Different forms of Flurbiprofen Sodium DMFs exist exist since differing nations have different regulations, such as Flurbiprofen Sodium USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Flurbiprofen Sodium DMF submitted to regulatory agencies in the US is known as a USDMF. Flurbiprofen Sodium USDMF includes data on Flurbiprofen Sodium's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Flurbiprofen Sodium USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Flurbiprofen Sodium 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 Flurbiprofen Sodium Drug Master File in Korea (Flurbiprofen Sodium KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Flurbiprofen Sodium. The MFDS reviews the Flurbiprofen Sodium KDMF as part of the drug registration process and uses the information provided in the Flurbiprofen Sodium KDMF to evaluate the safety and efficacy of the drug.
After submitting a Flurbiprofen Sodium 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 Flurbiprofen Sodium API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Flurbiprofen Sodium suppliers with KDMF on PharmaCompass.
A Flurbiprofen Sodium written confirmation (Flurbiprofen Sodium WC) is an official document issued by a regulatory agency to a Flurbiprofen Sodium manufacturer, verifying that the manufacturing facility of a Flurbiprofen Sodium active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Flurbiprofen Sodium APIs or Flurbiprofen Sodium finished pharmaceutical products to another nation, regulatory agencies frequently require a Flurbiprofen Sodium WC (written confirmation) as part of the regulatory process.
click here to find a list of Flurbiprofen Sodium suppliers with Written Confirmation (WC) on PharmaCompass.
Flurbiprofen Sodium 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 Flurbiprofen Sodium 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 Flurbiprofen Sodium GMP manufacturer or Flurbiprofen Sodium GMP API supplier for your needs.
A Flurbiprofen Sodium CoA (Certificate of Analysis) is a formal document that attests to Flurbiprofen Sodium's compliance with Flurbiprofen Sodium specifications and serves as a tool for batch-level quality control.
Flurbiprofen Sodium CoA mostly includes findings from lab analyses of a specific batch. For each Flurbiprofen Sodium 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.
Flurbiprofen Sodium may be tested according to a variety of international standards, such as European Pharmacopoeia (Flurbiprofen Sodium EP), Flurbiprofen Sodium JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Flurbiprofen Sodium USP).
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