Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
01 1SYMBIOTEC PHARMALAB PRIVATE LIMITED Indore IN
02 1ASPEN OSS B.V. Oss NL
03 1BAYER AG Leverkusen DE
04 1BEIJING KEYIFENG BIOTECH DEVELOPMENT CO. , LTD. Beijing CN
05 1GEDEON RICHTER PLC Budapest HU
06 1LA CHANDRA PHARMALAB PRIVATE LIMITED Ahmedabad IN
07 1PFIZER INC. New York City US
08 1SHAKTI LIFESCIENCE PRIVATE LIMITED Boisar IN
09 2Shaanxi Hanjiang Pharmaceutical Group Co., Ltd. Hanzhong CN
10 1VALDEPHARM Val de Reuil FR
11 1ZHEJIANG XIANJU PHARMACEUTICAL CO., LTD. Xianju CN
01 7Estradiol hemihydrate
02 2Estradiol hemihydrate, Micronised
03 1Estradiol hemihydrate, Micronised and non-micronised
04 1Estradiol hemihydrate, Micronised fine, non-micronised
05 1Estradiol hemihydrate, Process B
01 4China
02 1France
03 1Germany
04 1Hungary
05 2India
06 1Netherlands
07 1U.S.A
08 1Blank
01 1Expired
02 10Valid
03 1Withdrawn by Holder
Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
Estradiol Hemihydrate, Micronised
Certificate Number : R0-CEP 2020-067 - Rev 00
Status : Valid
Issue Date : 2022-05-05
Type : Chemical
Substance Number : 821
Aspen API. More than just an API.
Aspen API. More than just an API.
Certificate Number : R2-CEP 1995-001 - Rev 03
Status : Valid
Issue Date : 2014-01-30
Type : Chemical
Substance Number : 821
Certificate Number : R2-CEP 1995-017 - Rev 04
Status : Valid
Issue Date : 2017-03-01
Type : Chemical
Substance Number : 821
Estradiol Hemihydrate, Micronised Fine, Non-micr...
Certificate Number : CEP 2009-241 - Rev 06
Status : Valid
Issue Date : 2023-09-20
Type : Chemical
Substance Number : 821
Certificate Number : R1-CEP 1999-040 - Rev 04
Status : Valid
Issue Date : 2014-08-12
Type : Chemical
Substance Number : 821
Estradiol Hemihydrate, Process B
Certificate Number : CEP 2023-179 - Rev 00
Status : Valid
Issue Date : 2024-09-25
Type : Chemical
Substance Number : 821
Certificate Number : CEP 2017-237 - Rev 01
Status : Valid
Issue Date : 2024-08-19
Type : Chemical
Substance Number : 821
Certificate Number : CEP 2022-286 - Rev 00
Status : Valid
Issue Date : 2024-08-20
Type : Chemical
Substance Number : 821
Estradiol Hemihydrate, Micronised And Non-micron...
Certificate Number : CEP 2022-220 - Rev 01
Status : Valid
Issue Date : 2024-06-25
Type : Chemical
Substance Number : 821
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Estradiol Hemihydrate, Micronised
Certificate Number : CEP 2023-379 - Rev 00
Status : Valid
Issue Date : 2024-12-11
Type : Chemical
Substance Number : 821
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
A Estradiol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Estradiol, including repackagers and relabelers. The FDA regulates Estradiol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Estradiol 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 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Estradiol supplier is an individual or a company that provides Estradiol active pharmaceutical ingredient (API) or Estradiol finished formulations upon request. The Estradiol suppliers may include Estradiol API manufacturers, exporters, distributors and traders.
click here to find a list of Estradiol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Estradiol CEP of the European Pharmacopoeia monograph is often referred to as a Estradiol Certificate of Suitability (COS). The purpose of a Estradiol CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Estradiol EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Estradiol to their clients by showing that a Estradiol CEP has been issued for it. The manufacturer submits a Estradiol CEP (COS) as part of the market authorization procedure, and it takes on the role of a Estradiol CEP holder for the record. Additionally, the data presented in the Estradiol CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Estradiol DMF.
A Estradiol CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Estradiol 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 suppliers with CEP (COS) on PharmaCompass.
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