01 1ICROM S.R.L. Concorezzo IT
01 1Fluorescein Sodium
01 1Italy
01 1Valid
Certificate Number : R1-CEP 2017-121 - Rev 00
Status : Valid
Issue Date : 2023-07-03
Type : Chemical
Substance Number : 1213
85
PharmaCompass offers a list of Fluorescein 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 Fluorescein manufacturer or Fluorescein supplier for your needs.
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PharmaCompass also assists you with knowing the Fluorescein API Price utilized in the formulation of products. Fluorescein API Price is not always fixed or binding as the Fluorescein Price is obtained through a variety of data sources. The Fluorescein Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Fluor I Strip A.T. manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fluor I Strip A.T., including repackagers and relabelers. The FDA regulates Fluor I Strip A.T. manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fluor I Strip A.T. API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Fluor I Strip A.T. supplier is an individual or a company that provides Fluor I Strip A.T. active pharmaceutical ingredient (API) or Fluor I Strip A.T. finished formulations upon request. The Fluor I Strip A.T. suppliers may include Fluor I Strip A.T. API manufacturers, exporters, distributors and traders.
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A Fluor I Strip A.T. CEP of the European Pharmacopoeia monograph is often referred to as a Fluor I Strip A.T. Certificate of Suitability (COS). The purpose of a Fluor I Strip A.T. CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Fluor I Strip A.T. EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Fluor I Strip A.T. to their clients by showing that a Fluor I Strip A.T. CEP has been issued for it. The manufacturer submits a Fluor I Strip A.T. CEP (COS) as part of the market authorization procedure, and it takes on the role of a Fluor I Strip A.T. CEP holder for the record. Additionally, the data presented in the Fluor I Strip A.T. CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Fluor I Strip A.T. DMF.
A Fluor I Strip A.T. CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Fluor I Strip A.T. CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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