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NDC API
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FDF
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Data Compilation #PharmaFlow
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API SUPPLIERS
IKF/Pharmasynthese have been with fine chemicals market and APIs performance for more than 40 years.
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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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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 Spasmaverine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Spasmaverine, including repackagers and relabelers. The FDA regulates Spasmaverine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Spasmaverine 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 Spasmaverine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Spasmaverine supplier is an individual or a company that provides Spasmaverine active pharmaceutical ingredient (API) or Spasmaverine finished formulations upon request. The Spasmaverine suppliers may include Spasmaverine API manufacturers, exporters, distributors and traders.
click here to find a list of Spasmaverine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Spasmaverine DMF (Drug Master File) is a document detailing the whole manufacturing process of Spasmaverine active pharmaceutical ingredient (API) in detail. Different forms of Spasmaverine DMFs exist exist since differing nations have different regulations, such as Spasmaverine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Spasmaverine DMF submitted to regulatory agencies in the US is known as a USDMF. Spasmaverine USDMF includes data on Spasmaverine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Spasmaverine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Spasmaverine 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 Spasmaverine Drug Master File in Korea (Spasmaverine KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Spasmaverine. The MFDS reviews the Spasmaverine KDMF as part of the drug registration process and uses the information provided in the Spasmaverine KDMF to evaluate the safety and efficacy of the drug.
After submitting a Spasmaverine 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 Spasmaverine API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Spasmaverine suppliers with KDMF on PharmaCompass.
Spasmaverine 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 Spasmaverine 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 Spasmaverine GMP manufacturer or Spasmaverine GMP API supplier for your needs.
A Spasmaverine CoA (Certificate of Analysis) is a formal document that attests to Spasmaverine's compliance with Spasmaverine specifications and serves as a tool for batch-level quality control.
Spasmaverine CoA mostly includes findings from lab analyses of a specific batch. For each Spasmaverine 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.
Spasmaverine may be tested according to a variety of international standards, such as European Pharmacopoeia (Spasmaverine EP), Spasmaverine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Spasmaverine USP).
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