Chirogate is a professional Prostaglandin manufacturer.
01 1Chirogate International Inc.
02 1Chirogate International Inc. Wulin Plant
03 2Piramal Healthcare UK Ltd.
04 1YS Life Science Co., Ltd.
Chirogate is a professional Prostaglandin manufacturer.
Registrant Name : 신풍제약(주)
Registration Date : 2022-01-14
Registration Number : 20220114-209-J-1214
Manufacturer Name : Chirogate International Inc.
Manufacturer Address : No.41, Lane 298, Gong 2nd Rd., and No.22, Alley 39, Lane 298, Gong 2nd Rd., Longtan D...
Chirogate is a professional Prostaglandin manufacturer.
Registrant Name : Unimed Pharmaceutical Co., Ltd.
Registration Date : 2021-10-05
Registration Number : 20211005-209-J-1115
Manufacturer Name : Chirogate International Inc....
Manufacturer Address : No. 41, Sec. 1, Gong 2nd Rd., and No. 22, Alley 39, Sec.1, Gong 2nd Rd., Longtan Dist...
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PharmaCompass offers a list of Misoprostol 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 Misoprostol manufacturer or Misoprostol supplier for your needs.
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A 59122-46-2 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 59122-46-2, including repackagers and relabelers. The FDA regulates 59122-46-2 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 59122-46-2 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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A 59122-46-2 supplier is an individual or a company that provides 59122-46-2 active pharmaceutical ingredient (API) or 59122-46-2 finished formulations upon request. The 59122-46-2 suppliers may include 59122-46-2 API manufacturers, exporters, distributors and traders.
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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 59122-46-2 Drug Master File in Korea (59122-46-2 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of 59122-46-2. The MFDS reviews the 59122-46-2 KDMF as part of the drug registration process and uses the information provided in the 59122-46-2 KDMF to evaluate the safety and efficacy of the drug.
After submitting a 59122-46-2 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 59122-46-2 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of 59122-46-2 suppliers with KDMF on PharmaCompass.
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