01 2Merck Serono S. A.
01 2Cetuximab concentrated bulk
01 2Germany
Registration Number : 301MF10063
Registrant's Address : Zone industriale de l'Auriettaz, Rue de l'Auriette 151, 1170 Aubonne, Switzerland
Initial Date of Registration : 2019-09-11
Latest Date of Registration : 2020-08-05
Registration Number : 305MF10129
Registrant's Address : Zone industriale de l'Auriettaz, Rue de l'Auriette 151, 1170 Aubonne, Switzerland
Initial Date of Registration : 2023-12-06
Latest Date of Registration : 2023-12-06
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PharmaCompass offers a list of Cetuximab 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 Cetuximab manufacturer or Cetuximab supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cetuximab manufacturer or Cetuximab supplier.
PharmaCompass also assists you with knowing the Cetuximab API Price utilized in the formulation of products. Cetuximab API Price is not always fixed or binding as the Cetuximab Price is obtained through a variety of data sources. The Cetuximab Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A ERBITUX manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ERBITUX, including repackagers and relabelers. The FDA regulates ERBITUX manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ERBITUX 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 ERBITUX manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A ERBITUX supplier is an individual or a company that provides ERBITUX active pharmaceutical ingredient (API) or ERBITUX finished formulations upon request. The ERBITUX suppliers may include ERBITUX API manufacturers, exporters, distributors and traders.
click here to find a list of ERBITUX 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 ERBITUX Drug Master File in Japan (ERBITUX JDMF) empowers ERBITUX 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 ERBITUX JDMF during the approval evaluation for pharmaceutical products. At the time of ERBITUX 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 ERBITUX suppliers with JDMF on PharmaCompass.
