01 1Hetero Labs Limited
01 1Sorafenib tosylate [D]
01 1India
Registration Number : 230MF10114
Registrant's Address : 7-2-A2,Hetero Corporate,Industrial Estates Sanath Nagar,Hyderabad-500 018 Telangana I...
Initial Date of Registration : 2018-08-22
Latest Date of Registration : 2018-08-22
A Sorafenib Tosylate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sorafenib Tosylate, including repackagers and relabelers. The FDA regulates Sorafenib Tosylate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sorafenib Tosylate 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 Sorafenib Tosylate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sorafenib Tosylate supplier is an individual or a company that provides Sorafenib Tosylate active pharmaceutical ingredient (API) or Sorafenib Tosylate finished formulations upon request. The Sorafenib Tosylate suppliers may include Sorafenib Tosylate API manufacturers, exporters, distributors and traders.
click here to find a list of Sorafenib Tosylate 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 Sorafenib Tosylate Drug Master File in Japan (Sorafenib Tosylate JDMF) empowers Sorafenib Tosylate 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 Sorafenib Tosylate JDMF during the approval evaluation for pharmaceutical products. At the time of Sorafenib Tosylate 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 Sorafenib Tosylate suppliers with JDMF on PharmaCompass.
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