01 1Ranke Quimica S. A.
01 1Aclidinium bromide
01 1Spain
Registration Number : 226MF10012
Registrant's Address : General Miter, 151, 08022 Barcelona, Spain
Initial Date of Registration : 2014-01-08
Latest Date of Registration : 2023-01-11
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PharmaCompass offers a list of Aclidinium Bromide 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 Aclidinium Bromide manufacturer or Aclidinium Bromide supplier for your needs.
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PharmaCompass also assists you with knowing the Aclidinium Bromide API Price utilized in the formulation of products. Aclidinium Bromide API Price is not always fixed or binding as the Aclidinium Bromide Price is obtained through a variety of data sources. The Aclidinium Bromide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Eklira genuair (TN) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Eklira genuair (TN), including repackagers and relabelers. The FDA regulates Eklira genuair (TN) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Eklira genuair (TN) API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Eklira genuair (TN) supplier is an individual or a company that provides Eklira genuair (TN) active pharmaceutical ingredient (API) or Eklira genuair (TN) finished formulations upon request. The Eklira genuair (TN) suppliers may include Eklira genuair (TN) API manufacturers, exporters, distributors and traders.
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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 Eklira genuair (TN) Drug Master File in Japan (Eklira genuair (TN) JDMF) empowers Eklira genuair (TN) 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 Eklira genuair (TN) JDMF during the approval evaluation for pharmaceutical products. At the time of Eklira genuair (TN) JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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