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.
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
Aspen API. More than just an API™
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
Aspen API. More than just an API™
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
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PharmaCompass offers a list of Budesonide 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 Budesonide manufacturer or Budesonide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Budesonide manufacturer or Budesonide supplier.
PharmaCompass also assists you with knowing the Budesonide API Price utilized in the formulation of products. Budesonide API Price is not always fixed or binding as the Budesonide Price is obtained through a variety of data sources. The Budesonide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cortivent manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cortivent, including repackagers and relabelers. The FDA regulates Cortivent manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cortivent 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 Cortivent manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cortivent supplier is an individual or a company that provides Cortivent active pharmaceutical ingredient (API) or Cortivent finished formulations upon request. The Cortivent suppliers may include Cortivent API manufacturers, exporters, distributors and traders.
click here to find a list of Cortivent 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 Cortivent Drug Master File in Japan (Cortivent JDMF) empowers Cortivent 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 Cortivent JDMF during the approval evaluation for pharmaceutical products. At the time of Cortivent 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 Cortivent suppliers with JDMF on PharmaCompass.
We have 6 companies offering Cortivent
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