IKF/Pharmasynthese have been with fine chemicals market and APIs performance for more than 40 years.
01 1Pharmasynthesis SAS
02 1Zhejiang HISOAR Pharmaceutical Co. ,Ltd
01 1Amorolfine Hydrochloride
02 1Amorolfine hydrochloride (manufacturing only)
01 1China
02 1France
IKF/Pharmasynthese have been with fine chemicals market and APIs performance for more than 40 years.
Amorolfine hydrochloride (for manufacturing purposes only)
Registration Number : 303MF10079
Registrant's Address : 57, rue Gravetel St Pierre Les Elbeuf France
Initial Date of Registration : 2021-05-17
Latest Date of Registration : 2021-05-17
Registration Number : 303MF10111
Registrant's Address : No. 100 Waisha Branch Rd. , Jiaojiang, Taizhou, Zhejiang, China
Initial Date of Registration : 2021-07-16
Latest Date of Registration : 2021-07-16
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PharmaCompass also assists you with knowing the Amorolfine Hydrochloride API Price utilized in the formulation of products. Amorolfine Hydrochloride API Price is not always fixed or binding as the Amorolfine Hydrochloride Price is obtained through a variety of data sources. The Amorolfine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Amorolfin;Curanail;Loceryl;Locetar;Odenil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Amorolfin;Curanail;Loceryl;Locetar;Odenil, including repackagers and relabelers. The FDA regulates Amorolfin;Curanail;Loceryl;Locetar;Odenil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Amorolfin;Curanail;Loceryl;Locetar;Odenil 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 Amorolfin;Curanail;Loceryl;Locetar;Odenil supplier is an individual or a company that provides Amorolfin;Curanail;Loceryl;Locetar;Odenil active pharmaceutical ingredient (API) or Amorolfin;Curanail;Loceryl;Locetar;Odenil finished formulations upon request. The Amorolfin;Curanail;Loceryl;Locetar;Odenil suppliers may include Amorolfin;Curanail;Loceryl;Locetar;Odenil API manufacturers, exporters, distributors and traders.
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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 Amorolfin;Curanail;Loceryl;Locetar;Odenil Drug Master File in Japan (Amorolfin;Curanail;Loceryl;Locetar;Odenil JDMF) empowers Amorolfin;Curanail;Loceryl;Locetar;Odenil 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 Amorolfin;Curanail;Loceryl;Locetar;Odenil JDMF during the approval evaluation for pharmaceutical products. At the time of Amorolfin;Curanail;Loceryl;Locetar;Odenil JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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