Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
01 1Sochinaz SA
01 1Daewoong Pharmaceutical Co., Ltd.
01 1Revlan
01 1Switzerland
Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
Registrant Name : Daewoong Pharmaceutical Co., Ltd.
Registration Date : 2007-09-28
Registration Number : 43-2-ND
Manufacturer Name : Sochinaz SA
Manufacturer Address : Route du Simplon 22 CH-1895 Vionnaz, Switzerland
A Levulan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Levulan, including repackagers and relabelers. The FDA regulates Levulan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Levulan 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 Levulan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Levulan supplier is an individual or a company that provides Levulan active pharmaceutical ingredient (API) or Levulan finished formulations upon request. The Levulan suppliers may include Levulan API manufacturers, exporters, distributors and traders.
click here to find a list of Levulan 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 Levulan Drug Master File in Korea (Levulan KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Levulan. The MFDS reviews the Levulan KDMF as part of the drug registration process and uses the information provided in the Levulan KDMF to evaluate the safety and efficacy of the drug.
After submitting a Levulan 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 Levulan API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Levulan suppliers with KDMF on PharmaCompass.
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