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 offers a list of Amorolfine Hydrochloride 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 Amorolfine Hydrochloride manufacturer or Amorolfine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Amorolfine Hydrochloride manufacturer or Amorolfine Hydrochloride supplier.
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 Curanail manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Curanail, including repackagers and relabelers. The FDA regulates Curanail manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Curanail 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 Curanail manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Curanail supplier is an individual or a company that provides Curanail active pharmaceutical ingredient (API) or Curanail finished formulations upon request. The Curanail suppliers may include Curanail API manufacturers, exporters, distributors and traders.
click here to find a list of Curanail 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 Curanail Drug Master File in Japan (Curanail JDMF) empowers Curanail 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 Curanail JDMF during the approval evaluation for pharmaceutical products. At the time of Curanail 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 Curanail suppliers with JDMF on PharmaCompass.
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