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 : 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
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
55
PharmaCompass offers a list of Prednisolone Acetate 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 Prednisolone Acetate manufacturer or Prednisolone Acetate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Prednisolone Acetate manufacturer or Prednisolone Acetate supplier.
PharmaCompass also assists you with knowing the Prednisolone Acetate API Price utilized in the formulation of products. Prednisolone Acetate API Price is not always fixed or binding as the Prednisolone Acetate Price is obtained through a variety of data sources. The Prednisolone Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A CAS-52-21-1 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CAS-52-21-1, including repackagers and relabelers. The FDA regulates CAS-52-21-1 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CAS-52-21-1 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 CAS-52-21-1 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A CAS-52-21-1 supplier is an individual or a company that provides CAS-52-21-1 active pharmaceutical ingredient (API) or CAS-52-21-1 finished formulations upon request. The CAS-52-21-1 suppliers may include CAS-52-21-1 API manufacturers, exporters, distributors and traders.
click here to find a list of CAS-52-21-1 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 CAS-52-21-1 Drug Master File in Japan (CAS-52-21-1 JDMF) empowers CAS-52-21-1 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 CAS-52-21-1 JDMF during the approval evaluation for pharmaceutical products. At the time of CAS-52-21-1 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 CAS-52-21-1 suppliers with JDMF on PharmaCompass.
We have 2 companies offering CAS-52-21-1
Get in contact with the supplier of your choice:
