01 1Valdepharm
01 1Estradiol Valerate
01 1Luxembourg
Registration Number : 303MF10163
Registrant's Address : Parc Industriel d'Incarville Parc de la Fringale CS 10606 27106 Val de Reuil Cedex Fr...
Initial Date of Registration : 2021-11-10
Latest Date of Registration : 2022-09-14
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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.
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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.
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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.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Primogyna Drug Master File in Japan (Primogyna JDMF) empowers Primogyna API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Primogyna JDMF during the approval evaluation for pharmaceutical products. At the time of Primogyna JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Primogyna suppliers with JDMF on PharmaCompass.
