01 1BERNETT SRL Milano IT
02 2EUROMED S.A. Mollet del Vallès ES
03 1Finzelberg GmbH & Co. KG Andernach DE
04 1GREENTECH Saint-Beauzire FR
05 1NATUREX S.P.A. Caronno Pertusella IT
01 1Valerian dry aqueous extract, DER: 4-6:1
02 1Valerian dry hydroalcoholic extract, DER: 2.5-3.3:1
03 1Valerian dry hydroalcoholic extract, DER: 2.5-6/1
04 1Valerian dry hydroalcoholic extract, DER: 3-4:1
05 1Valerian dry hydroalcoholic extract, DER: 3-5:1
06 1Valerian dry hydroalcoholic extract, DER:3-6:1
01 2France
02 1Germany
03 1Italy
04 2Spain
01 1Expired
02 1Suspended by Holder
03 4Valid
Valerian Dry Hydroalcoholic Extract, DER: 3-4:1
Certificate Number : R1-CEP 2008-159 - Rev 00
Status : Valid
Issue Date : 2015-02-20
Type : Herbal
Substance Number : 1898
Valerian Dry Hydroalcoholic Extract, DER: 3-5:1
Certificate Number : R1-CEP 2013-186 - Rev 00
Status : Valid
Issue Date : 2019-03-27
Type : Herbal
Substance Number : 1898
Valerian Dry Aqueous Extract, DER: 4-6:1
Certificate Number : R1-CEP 2011-216 - Rev 00
Status : Valid
Issue Date : 2018-01-29
Type : Herbal
Substance Number : 2400
Valerian Dry Hydroalcoholic Extract, DER:3-6:1
Certificate Number : R1-CEP 2011-394 - Rev 00
Status : Valid
Issue Date : 2017-09-12
Type : Herbal
Substance Number : 1898
Valerian Dry Hydroalcoholic Extract, DER: 2.5-3....
Certificate Number : CEP 2011-229 - Rev 01
Status : Suspended by Holder
Issue Date : 2024-01-24
Type : Herbal
Substance Number : 1898
Valerian Dry Hydroalcoholic Extract, DER: 2.5-6/...
Certificate Number : R0-CEP 2013-137 - Rev 00
Status : Expired
Issue Date : 2014-07-08
Type : Herbal
Substance Number : 1898
31
PharmaCompass offers a list of Valeric Acid 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 Valeric Acid manufacturer or Valeric Acid supplier for your needs.
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A pentoate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of pentoate, including repackagers and relabelers. The FDA regulates pentoate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. pentoate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A pentoate supplier is an individual or a company that provides pentoate active pharmaceutical ingredient (API) or pentoate finished formulations upon request. The pentoate suppliers may include pentoate API manufacturers, exporters, distributors and traders.
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A pentoate CEP of the European Pharmacopoeia monograph is often referred to as a pentoate Certificate of Suitability (COS). The purpose of a pentoate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of pentoate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of pentoate to their clients by showing that a pentoate CEP has been issued for it. The manufacturer submits a pentoate CEP (COS) as part of the market authorization procedure, and it takes on the role of a pentoate CEP holder for the record. Additionally, the data presented in the pentoate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the pentoate DMF.
A pentoate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. pentoate 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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