01 1Chungking Carelife Pharmaceutical Co., Ltd.
01 1Mitoxantrone Hydrochloride
01 1China
Registration Number : 302MF10131
Registrant's Address : 3 Hua Nanyi Road Chongqing (Changshou) Chemical Industrial Park Chongqing 401254
Initial Date of Registration : 2020-10-26
Latest Date of Registration : 2020-10-26
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PharmaCompass offers a list of Mitoxantrone 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 Mitoxantrone manufacturer or Mitoxantrone supplier for your needs.
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PharmaCompass also assists you with knowing the Mitoxantrone API Price utilized in the formulation of products. Mitoxantrone API Price is not always fixed or binding as the Mitoxantrone Price is obtained through a variety of data sources. The Mitoxantrone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A DHAQ (*Diacetate salt*) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DHAQ (*Diacetate salt*), including repackagers and relabelers. The FDA regulates DHAQ (*Diacetate salt*) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DHAQ (*Diacetate salt*) 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 DHAQ (*Diacetate salt*) manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A DHAQ (*Diacetate salt*) supplier is an individual or a company that provides DHAQ (*Diacetate salt*) active pharmaceutical ingredient (API) or DHAQ (*Diacetate salt*) finished formulations upon request. The DHAQ (*Diacetate salt*) suppliers may include DHAQ (*Diacetate salt*) API manufacturers, exporters, distributors and traders.
click here to find a list of DHAQ (*Diacetate salt*) 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 DHAQ (*Diacetate salt*) Drug Master File in Japan (DHAQ (*Diacetate salt*) JDMF) empowers DHAQ (*Diacetate salt*) 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 DHAQ (*Diacetate salt*) JDMF during the approval evaluation for pharmaceutical products. At the time of DHAQ (*Diacetate salt*) 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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