01 2ABIOGEN PHARMA S.P.A. PISA IT
02 1PATHEON AUSTRIA GMBH & CO. KG Linz AT
03 1PharmaZell GmbH Raubling DE
01 3Clodronate disodium tetrahydrate
02 1Clodronate disodium tetrahydrate, Process 2
01 1Germany
02 2Italy
03 1U.S.A
01 3Valid
02 1Withdrawn by Holder
Clodronate Disodium Tetrahydrate, Process 2
Certificate Number : CEP 2023-215 - Rev 00
Status : Valid
Issue Date : 2024-09-30
Type : Chemical
Substance Number : 1777
Clodronate Disodium Tetrahydrate
Certificate Number : CEP 2018-078 - Rev 04
Status : Valid
Issue Date : 2024-08-30
Type : Chemical
Substance Number : 1777
Clodronate Disodium Tetrahydrate
Certificate Number : R1-CEP 2011-060 - Rev 00
Status : Valid
Issue Date : 2018-06-13
Type : Chemical
Substance Number : 1777
Clodronate Disodium Tetrahydrate
Certificate Number : R1-CEP 2009-095 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2015-11-03
Type : Chemical
Substance Number : 1777
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PharmaCompass offers a list of Clodronic Acid Disodium Salt 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 Clodronic Acid Disodium Salt manufacturer or Clodronic Acid Disodium Salt supplier for your needs.
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PharmaCompass also assists you with knowing the Clodronic Acid Disodium Salt API Price utilized in the formulation of products. Clodronic Acid Disodium Salt API Price is not always fixed or binding as the Clodronic Acid Disodium Salt Price is obtained through a variety of data sources. The Clodronic Acid Disodium Salt Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Bonefos manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bonefos, including repackagers and relabelers. The FDA regulates Bonefos manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bonefos 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 Bonefos supplier is an individual or a company that provides Bonefos active pharmaceutical ingredient (API) or Bonefos finished formulations upon request. The Bonefos suppliers may include Bonefos API manufacturers, exporters, distributors and traders.
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A Bonefos CEP of the European Pharmacopoeia monograph is often referred to as a Bonefos Certificate of Suitability (COS). The purpose of a Bonefos CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Bonefos EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Bonefos to their clients by showing that a Bonefos CEP has been issued for it. The manufacturer submits a Bonefos CEP (COS) as part of the market authorization procedure, and it takes on the role of a Bonefos CEP holder for the record. Additionally, the data presented in the Bonefos CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Bonefos DMF.
A Bonefos CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Bonefos 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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