01 1C-SQUARED PHARMA LIMITED Cork IE
02 1ESTEVE QUIMICA S.A. Barcelona ES
01 2Cyclopentolate hydrochloride
01 1Ireland
02 1Spain
01 2Valid
Certificate Number : R0-CEP 2021-469 - Rev 00
Status : Valid
Issue Date : 2023-06-05
Type : Chemical
Substance Number : 1093
Certificate Number : R1-CEP 2016-078 - Rev 00
Status : Valid
Issue Date : 2022-10-19
Type : Chemical
Substance Number : 1093
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PharmaCompass offers a list of Cyclopentolate Hydrochloride 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 Cyclopentolate Hydrochloride manufacturer or Cyclopentolate Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cyclopentolate Hydrochloride manufacturer or Cyclopentolate Hydrochloride supplier.
PharmaCompass also assists you with knowing the Cyclopentolate Hydrochloride API Price utilized in the formulation of products. Cyclopentolate Hydrochloride API Price is not always fixed or binding as the Cyclopentolate Hydrochloride Price is obtained through a variety of data sources. The Cyclopentolate Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cicloplegicedol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cicloplegicedol, including repackagers and relabelers. The FDA regulates Cicloplegicedol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cicloplegicedol 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 Cicloplegicedol supplier is an individual or a company that provides Cicloplegicedol active pharmaceutical ingredient (API) or Cicloplegicedol finished formulations upon request. The Cicloplegicedol suppliers may include Cicloplegicedol API manufacturers, exporters, distributors and traders.
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A Cicloplegicedol CEP of the European Pharmacopoeia monograph is often referred to as a Cicloplegicedol Certificate of Suitability (COS). The purpose of a Cicloplegicedol CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Cicloplegicedol EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Cicloplegicedol to their clients by showing that a Cicloplegicedol CEP has been issued for it. The manufacturer submits a Cicloplegicedol CEP (COS) as part of the market authorization procedure, and it takes on the role of a Cicloplegicedol CEP holder for the record. Additionally, the data presented in the Cicloplegicedol CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Cicloplegicedol DMF.
A Cicloplegicedol CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Cicloplegicedol 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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