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01 1QILU PHARMACEUTICAL CO., LTD. Jinan CN
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01 1Tropisetron hydrochloride
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01 1China
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01 1Withdrawn by Holder
Certificate Number : R1-CEP 2010-173 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2021-09-16
Type : Chemical
Substance Number : 2102
31
PharmaCompass offers a list of Tropisetron 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 Tropisetron hydrochloride manufacturer or Tropisetron hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Tropisetron hydrochloride API Price utilized in the formulation of products. Tropisetron hydrochloride API Price is not always fixed or binding as the Tropisetron hydrochloride Price is obtained through a variety of data sources. The Tropisetron hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Navoban manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Navoban, including repackagers and relabelers. The FDA regulates Navoban manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Navoban 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 Navoban supplier is an individual or a company that provides Navoban active pharmaceutical ingredient (API) or Navoban finished formulations upon request. The Navoban suppliers may include Navoban API manufacturers, exporters, distributors and traders.
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A Navoban CEP of the European Pharmacopoeia monograph is often referred to as a Navoban Certificate of Suitability (COS). The purpose of a Navoban CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Navoban EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Navoban to their clients by showing that a Navoban CEP has been issued for it. The manufacturer submits a Navoban CEP (COS) as part of the market authorization procedure, and it takes on the role of a Navoban CEP holder for the record. Additionally, the data presented in the Navoban CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Navoban DMF.
A Navoban CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Navoban 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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