Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
01 2PHARMACEUTICAL WORKS POLPHARMA S.A. Starogard Gdanski PL
02 1FLEMING LABORATORIES LIMITED Hyderabad IN
01 2Ibandronate sodium monohydrate
02 1Ibandronate sodium monohydrate, Type I
01 1India
02 2Poland
01 3Valid
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
Ibandronate Sodium Monohydrate
Certificate Number : R0-CEP 2022-073 - Rev 00
Status : Valid
Issue Date : 2023-02-20
Type : Chemical
Substance Number : 2771
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
Ibandronate Sodium Monohydrate, Type I
Certificate Number : R0-CEP 2023-077 - Rev 00
Status : Valid
Issue Date : 2023-06-30
Type : Chemical
Substance Number : 2771
Ibandronate Sodium Monohydrate
Certificate Number : CEP 2022-338 - Rev 00
Status : Valid
Issue Date : 2024-06-21
Type : Chemical
Substance Number : 2771
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PharmaCompass offers a list of Ibandronate Sodium 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 Ibandronate Sodium manufacturer or Ibandronate Sodium supplier for your needs.
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PharmaCompass also assists you with knowing the Ibandronate Sodium API Price utilized in the formulation of products. Ibandronate Sodium API Price is not always fixed or binding as the Ibandronate Sodium Price is obtained through a variety of data sources. The Ibandronate Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Boniva manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Boniva, including repackagers and relabelers. The FDA regulates Boniva manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Boniva 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 Boniva manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Boniva supplier is an individual or a company that provides Boniva active pharmaceutical ingredient (API) or Boniva finished formulations upon request. The Boniva suppliers may include Boniva API manufacturers, exporters, distributors and traders.
click here to find a list of Boniva suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Boniva CEP of the European Pharmacopoeia monograph is often referred to as a Boniva Certificate of Suitability (COS). The purpose of a Boniva CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Boniva EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Boniva to their clients by showing that a Boniva CEP has been issued for it. The manufacturer submits a Boniva CEP (COS) as part of the market authorization procedure, and it takes on the role of a Boniva CEP holder for the record. Additionally, the data presented in the Boniva CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Boniva DMF.
A Boniva CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Boniva 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 Boniva suppliers with CEP (COS) on PharmaCompass.
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