EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1EUROAPI FRANCE
02 2ZHEJIANG XIANJU PHARMACEUTICAL CO. , LTD.
01 1Prednisolone Acatete
02 1Prednisolone Acetate
03 1Prednisolone acetate
01 2China
02 1France
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Registration Number : 222MF10090
Registrant's Address : 82 Avenue Raspail 94250 Gentilly France
Initial Date of Registration : 2010-03-17
Latest Date of Registration : 2010-03-17
Registration Number : 227MF10269
Registrant's Address : No. 1 Xianyao Road, Xianju, Zhejiang, China
Initial Date of Registration : 2015-11-19
Latest Date of Registration : 2015-11-19
Registration Number : 304MF10022
Registrant's Address : No. 1 Xianyao Road, Xianju, Zhejiang, China
Initial Date of Registration : 2022-01-26
Latest Date of Registration : 2023-03-15
A Prednisolone Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prednisolone Acetate, including repackagers and relabelers. The FDA regulates Prednisolone Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prednisolone Acetate 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 Prednisolone Acetate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Prednisolone Acetate supplier is an individual or a company that provides Prednisolone Acetate active pharmaceutical ingredient (API) or Prednisolone Acetate finished formulations upon request. The Prednisolone Acetate suppliers may include Prednisolone Acetate API manufacturers, exporters, distributors and traders.
click here to find a list of Prednisolone Acetate 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 Prednisolone Acetate Drug Master File in Japan (Prednisolone Acetate JDMF) empowers Prednisolone Acetate 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 Prednisolone Acetate JDMF during the approval evaluation for pharmaceutical products. At the time of Prednisolone Acetate 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 Prednisolone Acetate suppliers with JDMF on PharmaCompass.
We have 2 companies offering Prednisolone Acetate
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