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Status : Withdrawn by Holder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 Clodron manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Clodron, including repackagers and relabelers. The FDA regulates Clodron manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Clodron API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Clodron manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Clodron supplier is an individual or a company that provides Clodron active pharmaceutical ingredient (API) or Clodron finished formulations upon request. The Clodron suppliers may include Clodron API manufacturers, exporters, distributors and traders.
click here to find a list of Clodron suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Clodron CEP of the European Pharmacopoeia monograph is often referred to as a Clodron Certificate of Suitability (COS). The purpose of a Clodron CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Clodron EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Clodron to their clients by showing that a Clodron CEP has been issued for it. The manufacturer submits a Clodron CEP (COS) as part of the market authorization procedure, and it takes on the role of a Clodron CEP holder for the record. Additionally, the data presented in the Clodron CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Clodron DMF.
A Clodron CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Clodron 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 Clodron suppliers with CEP (COS) on PharmaCompass.
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