01 1Glenmark Life Sciences Limited.
02 1ORIL Industry
01 1Korea Serviette Co., Ltd.
02 1Sangjin Corporation
01 2Perindopril tertiary butylamine
01 1France
02 1India
Perindopril tertiary butylamine
Registrant Name : Sangjin Corporation
Registration Date : 2021-05-04
Registration Number : 20210504-209-J-856
Manufacturer Name : Glenmark Life Sciences Limit...
Manufacturer Address : Plot No 3109, GIDC Industrial Estate, Ankleshwar - 393 002, Dist. Bharuch, Gujarat St...
Perindopril tertiary butylamine
Registrant Name : Korea Serviette Co., Ltd.
Registration Date : 2022-01-03
Registration Number : 20220103-209-J-1190
Manufacturer Name : ORIL Industry
Manufacturer Address : 13, rue Auguste Desgenétais, BP 17, BOLBEC, 76210, France
75
PharmaCompass offers a list of Perindopril Erbumine 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 Perindopril Erbumine manufacturer or Perindopril Erbumine supplier for your needs.
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A AKOS015841351 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AKOS015841351, including repackagers and relabelers. The FDA regulates AKOS015841351 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AKOS015841351 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 AKOS015841351 supplier is an individual or a company that provides AKOS015841351 active pharmaceutical ingredient (API) or AKOS015841351 finished formulations upon request. The AKOS015841351 suppliers may include AKOS015841351 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 AKOS015841351 Drug Master File in Korea (AKOS015841351 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of AKOS015841351. The MFDS reviews the AKOS015841351 KDMF as part of the drug registration process and uses the information provided in the AKOS015841351 KDMF to evaluate the safety and efficacy of the drug.
After submitting a AKOS015841351 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 AKOS015841351 API can apply through the Korea Drug Master File (KDMF).
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