TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
01 1TAPI CZECH INDUSTRIES S.R.O. Opava CZ
02 2CHONGQING QIANTAI PHARMA CO., LTD. Chongqing CN
03 1Pharmacia & Upjohn SpA Milano IT
01 3Nicergoline
02 1Nicergoline, Taixing site
01 1Israel
02 1U.S.A
03 2Blank
01 1Expired
02 3Valid
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Certificate Number : CEP 2003-198 - Rev 05
Status : Valid
Issue Date : 2025-01-13
Type : Chemical
Substance Number : 1998
Certificate Number : R0-CEP 2001-107 - Rev 01
Status : Expired
Issue Date : 2005-03-10
Type : TSE
Substance Number : 1998
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Certificate Number : CEP 2023-311 - Rev 01
Status : Valid
Issue Date : 2025-02-07
Type : Chemical
Substance Number : 1998
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Website
Corporate PDF
Certificate Number : CEP 2022-026 - Rev 02
Status : Valid
Issue Date : 2025-03-19
Type : Chemical
Substance Number : 1998
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PharmaCompass offers a list of Nicergoline 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 Nicergoline manufacturer or Nicergoline supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Nicergoline manufacturer or Nicergoline supplier.
PharmaCompass also assists you with knowing the Nicergoline API Price utilized in the formulation of products. Nicergoline API Price is not always fixed or binding as the Nicergoline Price is obtained through a variety of data sources. The Nicergoline Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Sermion manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sermion, including repackagers and relabelers. The FDA regulates Sermion manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sermion 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 Sermion manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sermion supplier is an individual or a company that provides Sermion active pharmaceutical ingredient (API) or Sermion finished formulations upon request. The Sermion suppliers may include Sermion API manufacturers, exporters, distributors and traders.
click here to find a list of Sermion suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Sermion CEP of the European Pharmacopoeia monograph is often referred to as a Sermion Certificate of Suitability (COS). The purpose of a Sermion CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Sermion EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Sermion to their clients by showing that a Sermion CEP has been issued for it. The manufacturer submits a Sermion CEP (COS) as part of the market authorization procedure, and it takes on the role of a Sermion CEP holder for the record. Additionally, the data presented in the Sermion CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Sermion DMF.
A Sermion CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Sermion 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 Sermion suppliers with CEP (COS) on PharmaCompass.
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