Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
01 1ZAKŁADY FARMACEUTYCZNE POLPHARMA S.A. Starogard Gdański PL
02 1USV PRIVATE LIMITED Mumbai IN
03 1DR. REDDY'S LABORATORIES LIMITED Hyderabad IN
04 1EMCURE PHARMACEUTICALS LIMITED Pune IN
05 1HETERO LABS LIMITED Hyderabad IN
06 1HIKMA PHARMACEUTICALS LLC Amman JO
07 1JUBILANT PHARMOVA LIMITED Nanjangud IN
08 1SCINOPHARM TAIWAN, LTD. Shan-Hua TW
09 1SHANDONG NEW TIME PHARMACEUTICAL CO., LTD. Linyi CN
10 1SHILPA PHARMA LIFESCIENCES LIMITED Raichur IN
11 1TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL
01 11Zoledronic acid monohydrate
01 1China
02 1Gabon
03 5India
04 1Israel
05 1Poland
06 1Taiwan
07 1Blank
01 11Valid
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.
Certificate Number : CEP 2018-191 - Rev 03
Status : Valid
Issue Date : 2024-07-23
Type : Chemical
Substance Number : 2743
USV offers custom peptide synthesis ranging from gram to multi-gram to multi-kilogram quantities.
USV offers custom peptide synthesis ranging from gram to multi-gram to multi-kilogram quantities.
Certificate Number : R0-CEP 2022-203 - Rev 00
Status : Valid
Issue Date : 2023-02-10
Type : Chemical
Substance Number : 2743
Certificate Number : CEP 2020-205 - Rev 03
Status : Valid
Issue Date : 2024-09-03
Type : Chemical
Substance Number : 2743
Certificate Number : R0-CEP 2019-349 - Rev 01
Status : Valid
Issue Date : 2022-08-11
Type : Chemical
Substance Number : 2743
Certificate Number : R0-CEP 2021-177 - Rev 00
Status : Valid
Issue Date : 2022-08-26
Type : Chemical
Substance Number : 2743
Certificate Number : CEP 2019-281 - Rev 01
Status : Valid
Issue Date : 2024-10-16
Type : Chemical
Substance Number : 2743
Certificate Number : CEP 2021-269 - Rev 01
Status : Valid
Issue Date : 2024-10-04
Type : Chemical
Substance Number : 2743
Certificate Number : R0-CEP 2020-018 - Rev 01
Status : Valid
Issue Date : 2022-01-14
Type : Chemical
Substance Number : 2743
Certificate Number : CEP 2019-314 - Rev 01
Status : Valid
Issue Date : 2024-05-30
Type : Chemical
Substance Number : 2743
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Certificate Number : CEP 2023-275 - Rev 00
Status : Valid
Issue Date : 2024-12-13
Type : Chemical
Substance Number : 2743
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
A Zoledronic Acid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zoledronic Acid, including repackagers and relabelers. The FDA regulates Zoledronic Acid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zoledronic Acid 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 Zoledronic Acid manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zoledronic Acid supplier is an individual or a company that provides Zoledronic Acid active pharmaceutical ingredient (API) or Zoledronic Acid finished formulations upon request. The Zoledronic Acid suppliers may include Zoledronic Acid API manufacturers, exporters, distributors and traders.
click here to find a list of Zoledronic Acid suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Zoledronic Acid CEP of the European Pharmacopoeia monograph is often referred to as a Zoledronic Acid Certificate of Suitability (COS). The purpose of a Zoledronic Acid CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Zoledronic Acid EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Zoledronic Acid to their clients by showing that a Zoledronic Acid CEP has been issued for it. The manufacturer submits a Zoledronic Acid CEP (COS) as part of the market authorization procedure, and it takes on the role of a Zoledronic Acid CEP holder for the record. Additionally, the data presented in the Zoledronic Acid CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Zoledronic Acid DMF.
A Zoledronic Acid CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Zoledronic Acid 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 Zoledronic Acid suppliers with CEP (COS) on PharmaCompass.
We have 9 companies offering Zoledronic Acid
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