01 1Fine Chemicals Corporation (Pty) Limited
02 1GEDEON RICHTER Plc.
01 1Vincristine Sulfate
02 1Vincristine sulfate salt
01 1Hungary
02 1South Africa
Registration Number : 306MF10067
Registrant's Address : 15 Hawkins Avenue, Epping 1,7460, Cape Town, South Africa
Initial Date of Registration : 2024-05-15
Latest Date of Registration : 2024-05-15
Registration Number : 220MF10117
Registrant's Address : BUDAPEST, GYOMROI UT 19-21, HUNGARY
Initial Date of Registration : 2008-04-28
Latest Date of Registration : 2008-04-28
A Vincristine Sulfate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vincristine Sulfate, including repackagers and relabelers. The FDA regulates Vincristine Sulfate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vincristine Sulfate 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 Vincristine Sulfate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Vincristine Sulfate supplier is an individual or a company that provides Vincristine Sulfate active pharmaceutical ingredient (API) or Vincristine Sulfate finished formulations upon request. The Vincristine Sulfate suppliers may include Vincristine Sulfate API manufacturers, exporters, distributors and traders.
click here to find a list of Vincristine Sulfate 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 Vincristine Sulfate Drug Master File in Japan (Vincristine Sulfate JDMF) empowers Vincristine Sulfate 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 Vincristine Sulfate JDMF during the approval evaluation for pharmaceutical products. At the time of Vincristine Sulfate 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 Vincristine Sulfate suppliers with JDMF on PharmaCompass.
We have 2 companies offering Vincristine Sulfate
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
