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 Neofollin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Neofollin, including repackagers and relabelers. The FDA regulates Neofollin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Neofollin 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 Neofollin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Neofollin supplier is an individual or a company that provides Neofollin active pharmaceutical ingredient (API) or Neofollin finished formulations upon request. The Neofollin suppliers may include Neofollin API manufacturers, exporters, distributors and traders.
click here to find a list of Neofollin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Neofollin CEP of the European Pharmacopoeia monograph is often referred to as a Neofollin Certificate of Suitability (COS). The purpose of a Neofollin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Neofollin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Neofollin to their clients by showing that a Neofollin CEP has been issued for it. The manufacturer submits a Neofollin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Neofollin CEP holder for the record. Additionally, the data presented in the Neofollin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Neofollin DMF.
A Neofollin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Neofollin 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 Neofollin suppliers with CEP (COS) on PharmaCompass.
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