Minakem delivers API, HPAPI, steroids & CDMO services for generics with FDA/GMP certification, regulatory know-how & proven success.
01 1Minakem Dunkerque Production
02 2Aspen Oss B. V.
03 1INDUSTRIALE CHIMICA s. r. l.
04 1Newchem S. p. A.
05 1Sicor Societa (') Italiana Corticosteroidi S. r. l.
06 1Sicor de Me(´)xico,S. A. de C. V.
01 1BUDESONIDE
02 4Budesonide
03 1Budesonide "Teva 3"
04 1Budesonide "Teva"
01 1France
02 3Italy
03 1Mexico
04 2Netherlands
Minakem delivers API, HPAPI, steroids & CDMO services for generics with FDA/GMP certification, regulatory know-how & proven success.
Registration Number : 301MF10045
Registrant's Address : 224 avenue de la Dordogne Zone d'Entreprises du Nord Gracht 59640 Dunkerque, France
Initial Date of Registration : 2019-08-20
Latest Date of Registration : 2019-10-25
Registration Number : 305MF10040
Registrant's Address : Kloosterstraat 6, 5349 AB Oss, the Netherlands
Initial Date of Registration : 2023-03-29
Latest Date of Registration : 2023-03-29
Registration Number : 301MF10061
Registrant's Address : Kloosterstraat 6, 5349 AB Oss, the Netherlands
Initial Date of Registration : 2019-09-11
Latest Date of Registration : 2022-10-19
Registration Number : 229MF10129
Registrant's Address : Via E. H. Grieg, 13,21047 Saronno (VARESE) ITALY
Initial Date of Registration : 2017-07-14
Latest Date of Registration : 2017-07-14
Registration Number : 228MF10196
Registrant's Address : Via San Vittore, 39 - 20123 Milano (Italy)
Initial Date of Registration : 2016-10-17
Latest Date of Registration : 2016-10-17
Registration Number : 227MF10218
Registrant's Address : Av. San Rafael No. 35 Parque Industrial Lerma, CP52000 Lerma, Edo. Me(´)xico. MEXICO
Initial Date of Registration : 2015-08-31
Latest Date of Registration : 2016-09-02
Registration Number : 219MF10041
Registrant's Address : Piazzale Luigi Cadorna, 4-20123 MILANO, Italy
Initial Date of Registration : 2007-02-13
Latest Date of Registration : 2017-08-22
A Inflammide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Inflammide, including repackagers and relabelers. The FDA regulates Inflammide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Inflammide 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 Inflammide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Inflammide supplier is an individual or a company that provides Inflammide active pharmaceutical ingredient (API) or Inflammide finished formulations upon request. The Inflammide suppliers may include Inflammide API manufacturers, exporters, distributors and traders.
click here to find a list of Inflammide 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 Inflammide Drug Master File in Japan (Inflammide JDMF) empowers Inflammide 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 Inflammide JDMF during the approval evaluation for pharmaceutical products. At the time of Inflammide 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 Inflammide suppliers with JDMF on PharmaCompass.
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