01 1CARBOGEN AMCIS AG
02 1Lonza AG
01 2MAAA-1162a
01 1Switzerland
02 1U.S.A
Registration Number : 305MF10037
Registrant's Address : Hauptstrasse 171, CH-4416 Bubendorf, Switzerland
Initial Date of Registration : 2023-03-23
Latest Date of Registration : 2023-03-23
Registration Number : 305MF10036
Registrant's Address : Muenchensteiner strasse 38, CH-4002, Basel, Switzerland
Initial Date of Registration : 2023-03-23
Latest Date of Registration : 2023-03-23
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PharmaCompass offers a list of Deruxtecan 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 Deruxtecan manufacturer or Deruxtecan supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Deruxtecan manufacturer or Deruxtecan supplier.
PharmaCompass also assists you with knowing the Deruxtecan API Price utilized in the formulation of products. Deruxtecan API Price is not always fixed or binding as the Deruxtecan Price is obtained through a variety of data sources. The Deruxtecan Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Deruxtecan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Deruxtecan, including repackagers and relabelers. The FDA regulates Deruxtecan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Deruxtecan 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 Deruxtecan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Deruxtecan supplier is an individual or a company that provides Deruxtecan active pharmaceutical ingredient (API) or Deruxtecan finished formulations upon request. The Deruxtecan suppliers may include Deruxtecan API manufacturers, exporters, distributors and traders.
click here to find a list of Deruxtecan 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 Deruxtecan Drug Master File in Japan (Deruxtecan JDMF) empowers Deruxtecan 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 Deruxtecan JDMF during the approval evaluation for pharmaceutical products. At the time of Deruxtecan 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 Deruxtecan suppliers with JDMF on PharmaCompass.
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