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