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PharmaCompass offers a list of Copovidone 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 Copovidone manufacturer or Copovidone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Copovidone manufacturer or Copovidone supplier.
PharmaCompass also assists you with knowing the Copovidone API Price utilized in the formulation of products. Copovidone API Price is not always fixed or binding as the Copovidone Price is obtained through a variety of data sources. The Copovidone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Kollidon VA64 API manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Kollidon VA64 API, including repackagers and relabelers. The FDA regulates Kollidon VA64 API manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Kollidon VA64 API 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 Kollidon VA64 API supplier is an individual or a company that provides Kollidon VA64 API active pharmaceutical ingredient (API) or Kollidon VA64 API finished formulations upon request. The Kollidon VA64 API suppliers may include Kollidon VA64 API API manufacturers, exporters, distributors and traders.
click here to find a list of Kollidon VA64 API suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Kollidon VA64 API DMF (Drug Master File) is a document detailing the whole manufacturing process of Kollidon VA64 API active pharmaceutical ingredient (API) in detail. Different forms of Kollidon VA64 API DMFs exist exist since differing nations have different regulations, such as Kollidon VA64 API USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Kollidon VA64 API DMF submitted to regulatory agencies in the US is known as a USDMF. Kollidon VA64 API USDMF includes data on Kollidon VA64 API's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Kollidon VA64 API USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Kollidon VA64 API suppliers with USDMF on PharmaCompass.
A Kollidon VA64 API CEP of the European Pharmacopoeia monograph is often referred to as a Kollidon VA64 API Certificate of Suitability (COS). The purpose of a Kollidon VA64 API CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Kollidon VA64 API EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Kollidon VA64 API to their clients by showing that a Kollidon VA64 API CEP has been issued for it. The manufacturer submits a Kollidon VA64 API CEP (COS) as part of the market authorization procedure, and it takes on the role of a Kollidon VA64 API CEP holder for the record. Additionally, the data presented in the Kollidon VA64 API CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Kollidon VA64 API DMF.
A Kollidon VA64 API CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Kollidon VA64 API 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 Kollidon VA64 API suppliers with CEP (COS) on PharmaCompass.
Kollidon VA64 API 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 Kollidon VA64 API 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 Kollidon VA64 API GMP manufacturer or Kollidon VA64 API GMP API supplier for your needs.
A Kollidon VA64 API CoA (Certificate of Analysis) is a formal document that attests to Kollidon VA64 API's compliance with Kollidon VA64 API specifications and serves as a tool for batch-level quality control.
Kollidon VA64 API CoA mostly includes findings from lab analyses of a specific batch. For each Kollidon VA64 API 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.
Kollidon VA64 API may be tested according to a variety of international standards, such as European Pharmacopoeia (Kollidon VA64 API EP), Kollidon VA64 API JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Kollidon VA64 API USP).
