Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
01 1Chunghwa Chemical Synthesis & Biotech Co., Ltd. Shanjia Plant
02 1Astellas Pharma Inc. Toyama Technology Center
03 1Biocon Limited
04 2CONCORD BIOTECH LIMITED
05 1Chong Kun Dang Bio Co., Ltd.
06 1Chong Kun Dang Bio Co., Ltd._x000D_
07 1Joyang Laboratories
08 1Lee Yeon Pharmaceutical Co., Ltd.
09 1LifeCeutical
10 1North China Pharmaceutical Huasheng Co., Ltd
11 2Teva Czech Industries sro
Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
Registrant Name : Hwail Pharmaceutical Co., Ltd.
Registration Date : 2014-04-17
Registration Number : 20140417-204-I-289-08
Manufacturer Name : Chunghwa Chemical Synthesis ...
Manufacturer Address : No.1, Tung-Hsing st., Shu-Lin, New Taipei City, Taiwan
A Tacrolimus manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tacrolimus, including repackagers and relabelers. The FDA regulates Tacrolimus manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tacrolimus 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 Tacrolimus manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tacrolimus supplier is an individual or a company that provides Tacrolimus active pharmaceutical ingredient (API) or Tacrolimus finished formulations upon request. The Tacrolimus suppliers may include Tacrolimus API manufacturers, exporters, distributors and traders.
click here to find a list of Tacrolimus 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 Tacrolimus Drug Master File in Korea (Tacrolimus KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Tacrolimus. The MFDS reviews the Tacrolimus KDMF as part of the drug registration process and uses the information provided in the Tacrolimus KDMF to evaluate the safety and efficacy of the drug.
After submitting a Tacrolimus 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 Tacrolimus API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Tacrolimus suppliers with KDMF on PharmaCompass.
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