Veranova: A CDMO that manages complexity with confidence.
01 1VERANOVA, L.P. West Deptford US
02 1TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL
03 1CIPLA LIMITED Mumbai IN
04 1FRESENIUS KABI ONCOLOGY LIMITED Kalyani IN
05 1HERAEUS PRECIOUS METALS GMBH & CO. KG Hanau DE
06 1HETERO LABS LIMITED Hyderabad IN
07 1HOSPIRA BOULDER, INC. Boulder US
08 1KUNMING GUIYAN PHARMACEUTICAL CO., LTD. Kunming CN
09 1LABORATORIUM OFICHEM B.V. Ter Apel NL
10 1LAURUS LABS LIMITED Hyderabad IN
11 1MAC CHEM PRODUCTS (INDIA) PVT. LTD. Mumbai IN
12 1QILU PHARMACEUTICAL CO., LTD. Jinan CN
13 1SUN PHARMACEUTICAL INDUSTRIES LIMITED Mumbai IN
14 1UMICORE ARGENTINA S.A. Pilar Industrial Park AR
Veranova: A CDMO that manages complexity with confidence.
Certificate Number : CEP 2005-253 - Rev 01
Status : Valid
Issue Date : 2023-11-29
Type : Chemical
Substance Number : 599
TAPI offers customized CDMO Solutions for API development and manufacturing services.
Certificate Number : R1-CEP 2000-411 - Rev 03
Status : Valid
Issue Date : 2022-10-18
Type : Chemical
Substance Number : 599
A Cisplatin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cisplatin, including repackagers and relabelers. The FDA regulates Cisplatin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cisplatin 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 Cisplatin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cisplatin supplier is an individual or a company that provides Cisplatin active pharmaceutical ingredient (API) or Cisplatin finished formulations upon request. The Cisplatin suppliers may include Cisplatin API manufacturers, exporters, distributors and traders.
click here to find a list of Cisplatin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cisplatin CEP of the European Pharmacopoeia monograph is often referred to as a Cisplatin Certificate of Suitability (COS). The purpose of a Cisplatin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Cisplatin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Cisplatin to their clients by showing that a Cisplatin CEP has been issued for it. The manufacturer submits a Cisplatin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Cisplatin CEP holder for the record. Additionally, the data presented in the Cisplatin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Cisplatin DMF.
A Cisplatin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Cisplatin 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 Cisplatin suppliers with CEP (COS) on PharmaCompass.
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