01 1Zhejiang Hisun Pharmaceutical Co., Ltd.
01 1Ace Biopharm Co., Ltd.
01 1Ivermectin
01 1China
Registrant Name : Ace Biopharm Co., Ltd.
Registration Date : 2025-02-21
Registration Number : 20250221-211-J-1776
Manufacturer Name : Zhejiang Hisun Pharmaceutica...
Manufacturer Address : 56 Binhai Road, Jiaojiang District, Taizhou City, Zhejiang Province, People's Republi...
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A MK 933 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MK 933, including repackagers and relabelers. The FDA regulates MK 933 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MK 933 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 MK 933 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A MK 933 supplier is an individual or a company that provides MK 933 active pharmaceutical ingredient (API) or MK 933 finished formulations upon request. The MK 933 suppliers may include MK 933 API manufacturers, exporters, distributors and traders.
click here to find a list of MK 933 suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 MK 933 Drug Master File in Korea (MK 933 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of MK 933. The MFDS reviews the MK 933 KDMF as part of the drug registration process and uses the information provided in the MK 933 KDMF to evaluate the safety and efficacy of the drug.
After submitting a MK 933 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 MK 933 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of MK 933 suppliers with KDMF on PharmaCompass.
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