With Fermion, start the journey of your innovative API.
01 1Fermion Oy
02 1Jiangsu Hengrui Pharmaceuticals Co., Ltd
03 1Laurus Labs Private Limited
04 5Qilu Pharmaceutical Co., Ltd.
05 1ScinoPharm Taiwan, Ltd.
06 1Shandong Anxin Pharmaceutical Co., Ltd
07 1Shilpa Medicare Limited, Unit-1
08 1Shilpa Pharma Lifesciences Limited
With Fermion, start the journey of your innovative API.
Registrant Name : TNS
Registration Date : 2022-01-13
Registration Number : 20220113-210-J-1177
Manufacturer Name : Fermion Oy
Manufacturer Address : Laaketehtaantie 2, Oulu, FI-90660, Finland
A Irinotecan Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Irinotecan Hydrochloride, including repackagers and relabelers. The FDA regulates Irinotecan Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Irinotecan Hydrochloride 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 Irinotecan Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Irinotecan Hydrochloride supplier is an individual or a company that provides Irinotecan Hydrochloride active pharmaceutical ingredient (API) or Irinotecan Hydrochloride finished formulations upon request. The Irinotecan Hydrochloride suppliers may include Irinotecan Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Irinotecan Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Irinotecan Hydrochloride Drug Master File in Korea (Irinotecan Hydrochloride KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Irinotecan Hydrochloride. The MFDS reviews the Irinotecan Hydrochloride KDMF as part of the drug registration process and uses the information provided in the Irinotecan Hydrochloride KDMF to evaluate the safety and efficacy of the drug.
After submitting a Irinotecan Hydrochloride KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Irinotecan Hydrochloride API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Irinotecan Hydrochloride suppliers with KDMF on PharmaCompass.
We have 7 companies offering Irinotecan Hydrochloride
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