01 1Olon S. p. A.
01 1Cefazolin acid
01 1Italy
Registration Number : 219MF10322
Registrant's Address : Strada Rivoltana Km 6/7 20090 Rodano Milano Italy
Initial Date of Registration : 2007-10-24
Latest Date of Registration : 2020-01-17
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PharmaCompass offers a list of Cefazolin 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 Cefazolin manufacturer or Cefazolin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cefazolin manufacturer or Cefazolin supplier.
PharmaCompass also assists you with knowing the Cefazolin API Price utilized in the formulation of products. Cefazolin API Price is not always fixed or binding as the Cefazolin Price is obtained through a variety of data sources. The Cefazolin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cefamezin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cefamezin, including repackagers and relabelers. The FDA regulates Cefamezin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cefamezin 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 Cefamezin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cefamezin supplier is an individual or a company that provides Cefamezin active pharmaceutical ingredient (API) or Cefamezin finished formulations upon request. The Cefamezin suppliers may include Cefamezin API manufacturers, exporters, distributors and traders.
click here to find a list of Cefamezin 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 Cefamezin Drug Master File in Japan (Cefamezin JDMF) empowers Cefamezin 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 Cefamezin JDMF during the approval evaluation for pharmaceutical products. At the time of Cefamezin 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 Cefamezin suppliers with JDMF on PharmaCompass.
