EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1EUROAPI FRANCE
02 1Pfizer Inc.
01 1Hydrocortisone Acetate
02 1Hydrocortisone acetate
01 1France
02 1U.S.A
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Registration Number : 220MF10078
Registrant's Address : 15 rue Traversie(')re 75012 Paris France
Initial Date of Registration : 2008-03-14
Latest Date of Registration : 2019-08-20
Pfizer CentreOne is a global CDMO and a leading supplier of Specialty APIs.
Registration Number : 217MF10978
Registrant's Address : 235 East 42nd Street, New York, NY 10017
Initial Date of Registration : 2005-11-14
Latest Date of Registration : 2010-03-23
A Hydrocortisone Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hydrocortisone Acetate, including repackagers and relabelers. The FDA regulates Hydrocortisone Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hydrocortisone 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 Hydrocortisone Acetate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Hydrocortisone Acetate supplier is an individual or a company that provides Hydrocortisone Acetate active pharmaceutical ingredient (API) or Hydrocortisone Acetate finished formulations upon request. The Hydrocortisone Acetate suppliers may include Hydrocortisone Acetate API manufacturers, exporters, distributors and traders.
click here to find a list of Hydrocortisone 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 Hydrocortisone Acetate Drug Master File in Japan (Hydrocortisone Acetate JDMF) empowers Hydrocortisone 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 Hydrocortisone Acetate JDMF during the approval evaluation for pharmaceutical products. At the time of Hydrocortisone 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 Hydrocortisone Acetate suppliers with JDMF on PharmaCompass.
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