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.
click here to find a list of 59122-46-2 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 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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