Axplora- The partner of choice for complex APIs.
01 1Farmabios S. p. A.
02 1Alps Pharmaceutical Co., Ltd.
03 1Newchem S. p. A.
04 1STEROID S. p. A.
01 1Prednisolone Valerate Acetate
02 3Prednisolone valerate acetate
01 1Germany
02 2Italy
03 1Japan
Axplora- The partner of choice for complex APIs.
Registration Number : 221MF10010
Registrant's Address : Via Pavia, 1-27027 Gropello Cairoli, Pavia, Italy
Initial Date of Registration : 2009-01-13
Latest Date of Registration : 2009-01-13
Registration Number : 221MF10164
Registrant's Address : 2-10-50 Mukaimachi, Furukawa-cho, Hida-shi, Gifu Prefecture
Initial Date of Registration : 2009-07-23
Latest Date of Registration : 2009-07-23
Registration Number : 217MF11152
Registrant's Address : Via de Amicis 47, 20123 Milano, Italy
Initial Date of Registration : 2005-12-12
Latest Date of Registration : 2016-05-13
Registration Number : 217MF11303
Registrant's Address : Viale Spagna, 156 Cologno Monzese (MI) - ITALY
Initial Date of Registration : 2005-12-22
Latest Date of Registration : 2009-07-30
A Prednisolone Valerate Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prednisolone Valerate Acetate, including repackagers and relabelers. The FDA regulates Prednisolone Valerate Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prednisolone Valerate 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 Valerate Acetate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Prednisolone Valerate Acetate supplier is an individual or a company that provides Prednisolone Valerate Acetate active pharmaceutical ingredient (API) or Prednisolone Valerate Acetate finished formulations upon request. The Prednisolone Valerate Acetate suppliers may include Prednisolone Valerate Acetate API manufacturers, exporters, distributors and traders.
click here to find a list of Prednisolone Valerate 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 Valerate Acetate Drug Master File in Japan (Prednisolone Valerate Acetate JDMF) empowers Prednisolone Valerate 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 Valerate Acetate JDMF during the approval evaluation for pharmaceutical products. At the time of Prednisolone Valerate 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 Valerate Acetate suppliers with JDMF on PharmaCompass.
We have 4 companies offering Prednisolone Valerate Acetate
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