01 1Tianish Laboratories Private Limited
01 1Tofacitinib Citrate
01 1U.S.A
Registration Number : 305MF10124
Registrant's Address : Plot No. 564/A/22, Road No. 92, Jubilee Hills, Hyderabad-500096, Telangana, India
Initial Date of Registration : 2023-11-29
Latest Date of Registration : 2023-11-29
A Tasocitinib Citrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tasocitinib Citrate, including repackagers and relabelers. The FDA regulates Tasocitinib Citrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tasocitinib Citrate 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 Tasocitinib Citrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tasocitinib Citrate supplier is an individual or a company that provides Tasocitinib Citrate active pharmaceutical ingredient (API) or Tasocitinib Citrate finished formulations upon request. The Tasocitinib Citrate suppliers may include Tasocitinib Citrate API manufacturers, exporters, distributors and traders.
click here to find a list of Tasocitinib Citrate 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 Tasocitinib Citrate Drug Master File in Japan (Tasocitinib Citrate JDMF) empowers Tasocitinib Citrate 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 Tasocitinib Citrate JDMF during the approval evaluation for pharmaceutical products. At the time of Tasocitinib Citrate 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 Tasocitinib Citrate suppliers with JDMF on PharmaCompass.
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