Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
01 1PHARMACEUTICAL WORKS POLPHARMA S.A. Starogard Gdanski PL
02 1SUPRIYA LIFESCIENCE LTD. Mumbai IN
03 1HIKAL LIMITED Bangalore IN
04 1IPCA Laboratories Limited Mumbai IN
05 1SANECA PHARMACEUTICALS A.S. Hlohovec SK
06 1SINBIOTIK S.A. DE C.V. Tlalnepantla de Baz MX
07 1SOLARA ACTIVE PHARMA SCIENCES LIMITED Chennai IN
08 2SUN PHARMACEUTICAL INDUSTRIES LIMITED Mumbai IN
09 1ZENTIVA K.S. Praha 10 CZ
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
Certificate Number : R1-CEP 2004-246 - Rev 05
Status : Valid
Issue Date : 2023-01-27
Type : Chemical
Substance Number : 851
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Certificate Number : R0-CEP 2018-294 - Rev 00
Status : Valid
Issue Date : 2021-01-12
Type : Chemical
Substance Number : 851
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PharmaCompass offers a list of Pentoxifylline 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 Pentoxifylline manufacturer or Pentoxifylline supplier for your needs.
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A DSSTox_CID_3437 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DSSTox_CID_3437, including repackagers and relabelers. The FDA regulates DSSTox_CID_3437 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DSSTox_CID_3437 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A DSSTox_CID_3437 supplier is an individual or a company that provides DSSTox_CID_3437 active pharmaceutical ingredient (API) or DSSTox_CID_3437 finished formulations upon request. The DSSTox_CID_3437 suppliers may include DSSTox_CID_3437 API manufacturers, exporters, distributors and traders.
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A DSSTox_CID_3437 CEP of the European Pharmacopoeia monograph is often referred to as a DSSTox_CID_3437 Certificate of Suitability (COS). The purpose of a DSSTox_CID_3437 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of DSSTox_CID_3437 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of DSSTox_CID_3437 to their clients by showing that a DSSTox_CID_3437 CEP has been issued for it. The manufacturer submits a DSSTox_CID_3437 CEP (COS) as part of the market authorization procedure, and it takes on the role of a DSSTox_CID_3437 CEP holder for the record. Additionally, the data presented in the DSSTox_CID_3437 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the DSSTox_CID_3437 DMF.
A DSSTox_CID_3437 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. DSSTox_CID_3437 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 DSSTox_CID_3437 suppliers with CEP (COS) on PharmaCompass.
We have 9 companies offering DSSTox_CID_3437
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