01 1Lonza Biologics plc.
01 1hP67.6 antibody
01 1U.S.A
Registration Number : 218MF10401
Registrant's Address : 228 Bath Road, Slough, Berkshire SL1 4DX, UK
Initial Date of Registration : 2006-04-14
Latest Date of Registration : 2019-03-05
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PharmaCompass offers a list of Ozogamicin 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 Ozogamicin manufacturer or Ozogamicin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ozogamicin manufacturer or Ozogamicin supplier.
PharmaCompass also assists you with knowing the Ozogamicin API Price utilized in the formulation of products. Ozogamicin API Price is not always fixed or binding as the Ozogamicin Price is obtained through a variety of data sources. The Ozogamicin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ozogamicin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ozogamicin, including repackagers and relabelers. The FDA regulates Ozogamicin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ozogamicin API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Ozogamicin supplier is an individual or a company that provides Ozogamicin active pharmaceutical ingredient (API) or Ozogamicin finished formulations upon request. The Ozogamicin suppliers may include Ozogamicin API manufacturers, exporters, distributors and traders.
click here to find a list of Ozogamicin 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 Ozogamicin Drug Master File in Japan (Ozogamicin JDMF) empowers Ozogamicin 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 Ozogamicin JDMF during the approval evaluation for pharmaceutical products. At the time of Ozogamicin 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 Ozogamicin suppliers with JDMF on PharmaCompass.
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