IKF/Pharmasynthese have been with fine chemicals market and APIs performance for more than 40 years.
01 1Pharmasynthesis SAS
02 1GALEN-N Ltd.
01 1Esculoside
02 1Outsiders regulations esculoside (production only)
01 1Bulgaria
02 1France
IKF/Pharmasynthese have been with fine chemicals market and APIs performance for more than 40 years.
Extra-official regulation escroside (for manufacturing only)
Registration Number : 218MF10075
Registrant's Address : 57, rue Gravetel St Pierre Les Elbeuf, France
Initial Date of Registration : 2006-01-27
Latest Date of Registration : 2010-04-13
Registration Number : 305MF10119
Registrant's Address : No 23 Tvardishki prohod str. , office 4; P. B. 1404 Sofia, Republic of Bulgaria
Initial Date of Registration : 2023-11-01
Latest Date of Registration : 2023-11-01
A Esculin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Esculin, including repackagers and relabelers. The FDA regulates Esculin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Esculin 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 Esculin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Esculin supplier is an individual or a company that provides Esculin active pharmaceutical ingredient (API) or Esculin finished formulations upon request. The Esculin suppliers may include Esculin API manufacturers, exporters, distributors and traders.
click here to find a list of Esculin 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 Esculin Drug Master File in Japan (Esculin JDMF) empowers Esculin 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 Esculin JDMF during the approval evaluation for pharmaceutical products. At the time of Esculin 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 Esculin suppliers with JDMF on PharmaCompass.
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