01 1DYNAMIT NOBEL GmbH
01 1Ciclesonide
01 1Germany
Registration Number : 220MF10193
Registrant's Address : Kalkstrasse 218, 51377 Leverkusen, Germany
Initial Date of Registration : 2008-08-28
Latest Date of Registration : 2023-10-04
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PharmaCompass offers a list of Ciclesonide 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 Ciclesonide manufacturer or Ciclesonide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ciclesonide manufacturer or Ciclesonide supplier.
PharmaCompass also assists you with knowing the Ciclesonide API Price utilized in the formulation of products. Ciclesonide API Price is not always fixed or binding as the Ciclesonide Price is obtained through a variety of data sources. The Ciclesonide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Omnair manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Omnair, including repackagers and relabelers. The FDA regulates Omnair manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Omnair 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 Omnair manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Omnair supplier is an individual or a company that provides Omnair active pharmaceutical ingredient (API) or Omnair finished formulations upon request. The Omnair suppliers may include Omnair API manufacturers, exporters, distributors and traders.
click here to find a list of Omnair 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 Omnair Drug Master File in Japan (Omnair JDMF) empowers Omnair 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 Omnair JDMF during the approval evaluation for pharmaceutical products. At the time of Omnair 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 Omnair suppliers with JDMF on PharmaCompass.
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