01 1Siegfried Ltd.
01 1Ildong Pharmaceutical Co., Ltd.
01 1Locaserin hydrochloride hydrate
01 1Switzerland
Locaserin hydrochloride hydrate
Registrant Name : Ildong Pharmaceutical Co., Ltd.
Registration Date : 2014-10-28
Registration Number : Number 2471-6-ND
Manufacturer Name : Siegfried Ltd.
Manufacturer Address : Untere Bruhlstrasse 4, 4800 Zofingen, Switzerland_x000D_
52
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A APD 356 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of APD 356, including repackagers and relabelers. The FDA regulates APD 356 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. APD 356 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 APD 356 supplier is an individual or a company that provides APD 356 active pharmaceutical ingredient (API) or APD 356 finished formulations upon request. The APD 356 suppliers may include APD 356 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 APD 356 Drug Master File in Korea (APD 356 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of APD 356. The MFDS reviews the APD 356 KDMF as part of the drug registration process and uses the information provided in the APD 356 KDMF to evaluate the safety and efficacy of the drug.
After submitting a APD 356 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 APD 356 API can apply through the Korea Drug Master File (KDMF).
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