Aspen API. More than just an API.
01 1ASPEN OSS B.V. Oss NL
02 1BAYER AG Leverkusen DE
03 1SHAKTI LIFESCIENCE PRIVATE LIMITED Mumbai IN
04 1VALDEPHARM Val de Reuil FR
01 2Estradiol valerate
02 1Estradiol valerate, Micronised (micro 20)
03 1Estradiol valerate, Micronised fine, non-micronised
01 1France
02 1Germany
03 1India
04 1Netherlands
01 4Valid
Certificate Number : R1-CEP 2009-171 - Rev 01
Status : Valid
Issue Date : 2016-07-15
Type : Chemical
Substance Number : 1614
Estradiol Valerate, Micronised (micro 20)
Certificate Number : CEP 2006-166 - Rev 04
Status : Valid
Issue Date : 2024-10-09
Type : Chemical
Substance Number : 1614
Estradiol Valerate, Micronised Fine, Non-microni...
Certificate Number : CEP 2010-224 - Rev 05
Status : Valid
Issue Date : 2024-06-20
Type : Chemical
Substance Number : 1614
Certificate Number : CEP 2022-351 - Rev 00
Status : Valid
Issue Date : 2024-09-18
Type : Chemical
Substance Number : 1614
A Estradiol Valerate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Estradiol Valerate, including repackagers and relabelers. The FDA regulates Estradiol Valerate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Estradiol Valerate 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 Estradiol Valerate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Estradiol Valerate supplier is an individual or a company that provides Estradiol Valerate active pharmaceutical ingredient (API) or Estradiol Valerate finished formulations upon request. The Estradiol Valerate suppliers may include Estradiol Valerate API manufacturers, exporters, distributors and traders.
click here to find a list of Estradiol Valerate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Estradiol Valerate CEP of the European Pharmacopoeia monograph is often referred to as a Estradiol Valerate Certificate of Suitability (COS). The purpose of a Estradiol Valerate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Estradiol Valerate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Estradiol Valerate to their clients by showing that a Estradiol Valerate CEP has been issued for it. The manufacturer submits a Estradiol Valerate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Estradiol Valerate CEP holder for the record. Additionally, the data presented in the Estradiol Valerate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Estradiol Valerate DMF.
A Estradiol Valerate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Estradiol Valerate 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 Estradiol Valerate suppliers with CEP (COS) on PharmaCompass.
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