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PharmaCompass offers a list of Buflomedil 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 Buflomedil manufacturer or Buflomedil supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Buflomedil manufacturer or Buflomedil supplier.
PharmaCompass also assists you with knowing the Buflomedil API Price utilized in the formulation of products. Buflomedil API Price is not always fixed or binding as the Buflomedil Price is obtained through a variety of data sources. The Buflomedil Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Buflan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Buflan, including repackagers and relabelers. The FDA regulates Buflan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Buflan 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 Buflan supplier is an individual or a company that provides Buflan active pharmaceutical ingredient (API) or Buflan finished formulations upon request. The Buflan suppliers may include Buflan API manufacturers, exporters, distributors and traders.
click here to find a list of Buflan suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Buflan DMF (Drug Master File) is a document detailing the whole manufacturing process of Buflan active pharmaceutical ingredient (API) in detail. Different forms of Buflan DMFs exist exist since differing nations have different regulations, such as Buflan USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Buflan DMF submitted to regulatory agencies in the US is known as a USDMF. Buflan USDMF includes data on Buflan's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Buflan USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Buflan suppliers with USDMF on PharmaCompass.
A Buflan CEP of the European Pharmacopoeia monograph is often referred to as a Buflan Certificate of Suitability (COS). The purpose of a Buflan CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Buflan EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Buflan to their clients by showing that a Buflan CEP has been issued for it. The manufacturer submits a Buflan CEP (COS) as part of the market authorization procedure, and it takes on the role of a Buflan CEP holder for the record. Additionally, the data presented in the Buflan CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Buflan DMF.
A Buflan CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Buflan 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 Buflan suppliers with CEP (COS) on PharmaCompass.
Buflan 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 Buflan 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 Buflan GMP manufacturer or Buflan GMP API supplier for your needs.
A Buflan CoA (Certificate of Analysis) is a formal document that attests to Buflan's compliance with Buflan specifications and serves as a tool for batch-level quality control.
Buflan CoA mostly includes findings from lab analyses of a specific batch. For each Buflan 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.
Buflan may be tested according to a variety of international standards, such as European Pharmacopoeia (Buflan EP), Buflan JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Buflan USP).
