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NDC API
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Data Compilation #PharmaFlow
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ABOUT THIS PAGE
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PharmaCompass offers a list of Rescinnamine 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 Rescinnamine manufacturer or Rescinnamine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Rescinnamine manufacturer or Rescinnamine supplier.
PharmaCompass also assists you with knowing the Rescinnamine API Price utilized in the formulation of products. Rescinnamine API Price is not always fixed or binding as the Rescinnamine Price is obtained through a variety of data sources. The Rescinnamine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Moderil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Moderil, including repackagers and relabelers. The FDA regulates Moderil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Moderil API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Moderil supplier is an individual or a company that provides Moderil active pharmaceutical ingredient (API) or Moderil finished formulations upon request. The Moderil suppliers may include Moderil API manufacturers, exporters, distributors and traders.
click here to find a list of Moderil suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Moderil DMF (Drug Master File) is a document detailing the whole manufacturing process of Moderil active pharmaceutical ingredient (API) in detail. Different forms of Moderil DMFs exist exist since differing nations have different regulations, such as Moderil USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Moderil DMF submitted to regulatory agencies in the US is known as a USDMF. Moderil USDMF includes data on Moderil's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Moderil USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Moderil suppliers with USDMF on PharmaCompass.
Moderil 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 Moderil 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 Moderil GMP manufacturer or Moderil GMP API supplier for your needs.
A Moderil CoA (Certificate of Analysis) is a formal document that attests to Moderil's compliance with Moderil specifications and serves as a tool for batch-level quality control.
Moderil CoA mostly includes findings from lab analyses of a specific batch. For each Moderil 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.
Moderil may be tested according to a variety of international standards, such as European Pharmacopoeia (Moderil EP), Moderil JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Moderil USP).
