Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
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01 1PHARMACEUTICAL WORKS POLPHARMA S.A. Starogard Gdanski PL
02 1ZAKŁADY FARMACEUTYCZNE POLPHARMA S.A. Starogard Gdański PL
03 1AMOLI ORGANICS PRIVATE LIMITED Mumbai IN
04 1ANDHRA ORGANICS LIMITED Pydibhimavaram Village IN
05 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
06 1AZICO BIOPHORE INDIA PRIVATE LIMITED Hyderabad IN
07 1CADILA PHARMACEUTICALS LIMITED Ankleshwar IN
08 1HETERO DRUGS LIMITED Hyderabad IN
09 1JINAN MINGXIN PHARMACEUTICAL CO., LTD. Zhangqiu City CN
10 1MACLEODS PHARMACEUTICALS LIMITED Mumbai IN
11 1MAPRIMED S.A. Buenos Aires AR
12 1MSN ORGANICS PRIVATE LIMITED Bibinagar Village IN
13 1PHALANX LABS PRIVATE LIMITED Hyderabad IN
14 1RAKS PHARMA PVT. LTD. Visakhapatnam IN
15 1RAKSHIT PHARMACEUTICALS LIMITED Anakapalli IN
16 1SICHUAN KELUN PHARMACEUTICAL CO., LTD. Qionglai CN
17 1SMS LIFESCIENCES INDIA LIMITED Hyderabad IN
18 1SMS PHARMACEUTICALS LIMITED Hyderabad IN
19 1TIANISH LABORATORIES PRIVATE LIMITED Hyderabad IN
20 1TORRENT PHARMACEUTICALS LIMITED Ahmedabad IN
21 1Zhejiang Jiuzhou Pharmaceutical Co., Ltd. Taizhou City CN
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01 19Sildenafil citrate
02 1Sildenafil citrate, Process A
03 1Sildenafil citrate, Process B, standard, milled and micronised
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01 1Argentina
02 3China
03 15India
04 2Poland
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01 2Expired
02 18Valid
03 1Withdrawn by Holder
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.
Sildenafil Citrate, Process B, Standard, Milled ...
Certificate Number : CEP 2013-073 - Rev 04
Status : Valid
Issue Date : 2024-11-19
Type : Chemical
Substance Number : 2270
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 : R1-CEP 2013-072 - Rev 02
Status : Valid
Issue Date : 2022-03-14
Type : Chemical
Substance Number : 2270
Certificate Number : CEP 2013-002 - Rev 01
Status : Valid
Issue Date : 2025-01-29
Type : Chemical
Substance Number : 2270
Certificate Number : R1-CEP 2013-219 - Rev 01
Status : Valid
Issue Date : 2021-12-13
Type : Chemical
Substance Number : 2270
Certificate Number : R1-CEP 2014-246 - Rev 00
Status : Valid
Issue Date : 2021-01-18
Type : Chemical
Substance Number : 2270
Certificate Number : R1-CEP 2014-361 - Rev 01
Status : Valid
Issue Date : 2023-01-10
Type : Chemical
Substance Number : 2270
Certificate Number : CEP 2022-249 - Rev 00
Status : Valid
Issue Date : 2024-02-28
Type : Chemical
Substance Number : 2270
Certificate Number : CEP 2012-317 - Rev 02
Status : Valid
Issue Date : 2025-03-05
Type : Chemical
Substance Number : 2270
Certificate Number : CEP 2013-346 - Rev 02
Status : Valid
Issue Date : 2024-10-04
Type : Chemical
Substance Number : 2270
Certificate Number : CEP 2013-332 - Rev 04
Status : Valid
Issue Date : 2023-09-22
Type : Chemical
Substance Number : 2270
47
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A UK 92480-10 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of UK 92480-10, including repackagers and relabelers. The FDA regulates UK 92480-10 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. UK 92480-10 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 UK 92480-10 supplier is an individual or a company that provides UK 92480-10 active pharmaceutical ingredient (API) or UK 92480-10 finished formulations upon request. The UK 92480-10 suppliers may include UK 92480-10 API manufacturers, exporters, distributors and traders.
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A UK 92480-10 CEP of the European Pharmacopoeia monograph is often referred to as a UK 92480-10 Certificate of Suitability (COS). The purpose of a UK 92480-10 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of UK 92480-10 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of UK 92480-10 to their clients by showing that a UK 92480-10 CEP has been issued for it. The manufacturer submits a UK 92480-10 CEP (COS) as part of the market authorization procedure, and it takes on the role of a UK 92480-10 CEP holder for the record. Additionally, the data presented in the UK 92480-10 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the UK 92480-10 DMF.
A UK 92480-10 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. UK 92480-10 CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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We have 20 companies offering UK 92480-10
Get in contact with the supplier of your choice: