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API SUPPLIERS
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USDMF
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IKF/Pharmasynthese have been with fine chemicals market and APIs performance for more than 40 years.
About the Company : Established in 1990, Inabata France, a part of the Inabata Group, used to export chemical and pharmaceutical products to Japan. In 2006, it acquired Pharmasynthèse. Today, Inabata...
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API Imports and Exports
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REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
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PharmaCompass offers a list of Alverine 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 Alverine manufacturer or Alverine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Alverine manufacturer or Alverine supplier.
PharmaCompass also assists you with knowing the Alverine API Price utilized in the formulation of products. Alverine API Price is not always fixed or binding as the Alverine Price is obtained through a variety of data sources. The Alverine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Alverine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Alverine, including repackagers and relabelers. The FDA regulates Alverine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Alverine 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 Alverine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Alverine supplier is an individual or a company that provides Alverine active pharmaceutical ingredient (API) or Alverine finished formulations upon request. The Alverine suppliers may include Alverine API manufacturers, exporters, distributors and traders.
click here to find a list of Alverine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Alverine DMF (Drug Master File) is a document detailing the whole manufacturing process of Alverine active pharmaceutical ingredient (API) in detail. Different forms of Alverine DMFs exist exist since differing nations have different regulations, such as Alverine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Alverine DMF submitted to regulatory agencies in the US is known as a USDMF. Alverine USDMF includes data on Alverine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Alverine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Alverine 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 Alverine Drug Master File in Korea (Alverine KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Alverine. The MFDS reviews the Alverine KDMF as part of the drug registration process and uses the information provided in the Alverine KDMF to evaluate the safety and efficacy of the drug.
After submitting a Alverine 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 Alverine API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Alverine suppliers with KDMF on PharmaCompass.
Alverine 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 Alverine 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 Alverine GMP manufacturer or Alverine GMP API supplier for your needs.
A Alverine CoA (Certificate of Analysis) is a formal document that attests to Alverine's compliance with Alverine specifications and serves as a tool for batch-level quality control.
Alverine CoA mostly includes findings from lab analyses of a specific batch. For each Alverine 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.
Alverine may be tested according to a variety of international standards, such as European Pharmacopoeia (Alverine EP), Alverine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Alverine USP).
