European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.
01 1ZAKŁADY FARMACEUTYCZNE POLPHARMA S.A. Starogard Gdański PL
02 1TAPI NL B.V. Amsterdam NL
03 1EMCURE PHARMACEUTICALS LIMITED Pune IN
04 1HETERO LABS LIMITED Hyderabad IN
05 1HIKMA PHARMACEUTICALS LLC Amman JO
06 1JUBILANT BIOSYS LIMITED Nanjangud IN
07 1SCINOPHARM TAIWAN, LTD. Shan-Hua TW
08 1SHANDONG NEW TIME PHARMACEUTICAL CO., LTD. Linyi CN
09 1SHILPA PHARMA LIFESCIENCES LIMITED Raichur IN
10 1USV PRIVATE LIMITED Mumbai IN
European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.
Certificate Number : CEP 2018-191 - Rev 03
Status : Valid
Issue Date : 2024-07-23
Type : Chemical
Substance Number : 2743
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Certificate Number : CEP 2020-018 - Rev 02
Status : Valid
Issue Date : 2025-02-28
Type : Chemical
Substance Number : 2743
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PharmaCompass offers a list of Zoledronic Acid 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 Zoledronic Acid manufacturer or Zoledronic Acid supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Zoledronic Acid manufacturer or Zoledronic Acid supplier.
PharmaCompass also assists you with knowing the Zoledronic Acid API Price utilized in the formulation of products. Zoledronic Acid API Price is not always fixed or binding as the Zoledronic Acid Price is obtained through a variety of data sources. The Zoledronic Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Orazol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Orazol, including repackagers and relabelers. The FDA regulates Orazol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Orazol 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 Orazol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Orazol supplier is an individual or a company that provides Orazol active pharmaceutical ingredient (API) or Orazol finished formulations upon request. The Orazol suppliers may include Orazol API manufacturers, exporters, distributors and traders.
click here to find a list of Orazol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Orazol CEP of the European Pharmacopoeia monograph is often referred to as a Orazol Certificate of Suitability (COS). The purpose of a Orazol CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Orazol EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Orazol to their clients by showing that a Orazol CEP has been issued for it. The manufacturer submits a Orazol CEP (COS) as part of the market authorization procedure, and it takes on the role of a Orazol CEP holder for the record. Additionally, the data presented in the Orazol CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Orazol DMF.
A Orazol CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Orazol 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 Orazol suppliers with CEP (COS) on PharmaCompass.
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