Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
01 1PCAS Ecully FR
02 1Ergypharm Mundolsheim FR
03 1SICHUAN XIELI PHARMACEUTICAL CO., LTD. Pengzhou CN
01 3Troxerutin
01 1China
02 2France
01 1Expired
02 2Valid
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
Certificate Number : R1-CEP 2005-263 - Rev 08
Status : Valid
Issue Date : 2022-09-19
Type : Chemical
Substance Number : 2133
Certificate Number : R1-CEP 2016-279 - Rev 00
Status : Valid
Issue Date : 2023-01-09
Type : Chemical
Substance Number : 2133
Certificate Number : R0-CEP 2006-153 - Rev 01
Status : Expired
Issue Date : 2010-05-18
Type : Chemical
Substance Number : 2133
52
PharmaCompass offers a list of Troxerutin 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 Troxerutin manufacturer or Troxerutin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Troxerutin manufacturer or Troxerutin supplier.
PharmaCompass also assists you with knowing the Troxerutin API Price utilized in the formulation of products. Troxerutin API Price is not always fixed or binding as the Troxerutin Price is obtained through a variety of data sources. The Troxerutin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Venoruton manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Venoruton, including repackagers and relabelers. The FDA regulates Venoruton manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Venoruton 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 Venoruton manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Venoruton supplier is an individual or a company that provides Venoruton active pharmaceutical ingredient (API) or Venoruton finished formulations upon request. The Venoruton suppliers may include Venoruton API manufacturers, exporters, distributors and traders.
click here to find a list of Venoruton suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Venoruton CEP of the European Pharmacopoeia monograph is often referred to as a Venoruton Certificate of Suitability (COS). The purpose of a Venoruton CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Venoruton EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Venoruton to their clients by showing that a Venoruton CEP has been issued for it. The manufacturer submits a Venoruton CEP (COS) as part of the market authorization procedure, and it takes on the role of a Venoruton CEP holder for the record. Additionally, the data presented in the Venoruton CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Venoruton DMF.
A Venoruton CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Venoruton 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 Venoruton suppliers with CEP (COS) on PharmaCompass.
We have 2 companies offering Venoruton
Get in contact with the supplier of your choice:
