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 1ALLESSA GMBH FRANKFURT DE
01 2Molsidomine
01 1Germany
02 1Poland
01 2Valid
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 2017-021 - Rev 01
Status : Valid
Issue Date : 2024-03-25
Type : Chemical
Substance Number : 1701
Certificate Number : CEP 2017-214 - Rev 01
Status : Valid
Issue Date : 2024-01-05
Type : Chemical
Substance Number : 1701
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PharmaCompass offers a list of Molsidomine 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 Molsidomine manufacturer or Molsidomine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Molsidomine manufacturer or Molsidomine supplier.
PharmaCompass also assists you with knowing the Molsidomine API Price utilized in the formulation of products. Molsidomine API Price is not always fixed or binding as the Molsidomine Price is obtained through a variety of data sources. The Molsidomine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Molsidomin Stada manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Molsidomin Stada, including repackagers and relabelers. The FDA regulates Molsidomin Stada manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Molsidomin Stada 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 Molsidomin Stada manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Molsidomin Stada supplier is an individual or a company that provides Molsidomin Stada active pharmaceutical ingredient (API) or Molsidomin Stada finished formulations upon request. The Molsidomin Stada suppliers may include Molsidomin Stada API manufacturers, exporters, distributors and traders.
click here to find a list of Molsidomin Stada suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Molsidomin Stada CEP of the European Pharmacopoeia monograph is often referred to as a Molsidomin Stada Certificate of Suitability (COS). The purpose of a Molsidomin Stada CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Molsidomin Stada EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Molsidomin Stada to their clients by showing that a Molsidomin Stada CEP has been issued for it. The manufacturer submits a Molsidomin Stada CEP (COS) as part of the market authorization procedure, and it takes on the role of a Molsidomin Stada CEP holder for the record. Additionally, the data presented in the Molsidomin Stada CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Molsidomin Stada DMF.
A Molsidomin Stada CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Molsidomin Stada 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 Molsidomin Stada suppliers with CEP (COS) on PharmaCompass.
We have 2 companies offering Molsidomin Stada
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