Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
01 2Cohance Lifesciences Limited
02 1SCI Pharmtech, Inc.
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
Registrant Name : Pharmapia Co., Ltd.
Registration Date : 2024-07-02
Registration Number : 20220517-211-J-1296(1)
Manufacturer Name : Cohance Lifesciences Limited
Manufacturer Address : RS 50/1, Mukteswarapuram Village, Jaggaiahpeta Mandal, Krishna District-521 175. Andh...
SCI Pharmtech offers high-quality, cost-effective APIs, advanced intermediates, & custom products with global expertise and precision.
Registrant Name : Insung Trading Co., Ltd.
Registration Date : 2024-03-13
Registration Number : 20240313-211-J-1568
Manufacturer Name : SCI Pharmtech, Inc.
Manufacturer Address : No.61, Ln.309, Haihu N. Rd., Luzhu Dist., Taoyuan City 33856, Taiwan
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
Registrant Name : Aging Life Science Co., Ltd.
Registration Date : 2022-05-17
Registration Number : 20220517-211-J-1296
Manufacturer Name : Cohance Lifesciences Limited
Manufacturer Address : RS 50/1, Mukteswarapuram Village, Jaggaiahpeta Mandal, Krishna District-521 175. Andh...
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PharmaCompass offers a list of Articaine Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Articaine Hydrochloride manufacturer or Articaine Hydrochloride supplier for your needs.
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A Articaine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Articaine Hydrochloride, including repackagers and relabelers. The FDA regulates Articaine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Articaine 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.
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In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Articaine Hydrochloride Drug Master File in Korea (Articaine Hydrochloride KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Articaine Hydrochloride. The MFDS reviews the Articaine Hydrochloride KDMF as part of the drug registration process and uses the information provided in the Articaine Hydrochloride KDMF to evaluate the safety and efficacy of the drug.
After submitting a Articaine 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 Articaine Hydrochloride API can apply through the Korea Drug Master File (KDMF).
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