01 1Sicor Societa' Italiana Corticosteroidi SRL@Valdepharm
01 1Bansen Co., Ltd.
01 1Nomegestrol acetate
01 1Italy
Registrant Name : Bansen Co., Ltd.
Registration Date : 2024-10-15
Registration Number : 20241015-209-J-1903
Manufacturer Name : Sicor Societa' Italiana Cort...
Manufacturer Address : Tenuta S. Alessandro 13048 Santhia (VC), Italy@Parc Industriel d'Incarville, Parc de ...
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PharmaCompass offers a list of Nomegestrol Acetate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Nomegestrol Acetate manufacturer or Nomegestrol Acetate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Nomegestrol Acetate manufacturer or Nomegestrol Acetate supplier.
A NomegestrolAcetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of NomegestrolAcetate, including repackagers and relabelers. The FDA regulates NomegestrolAcetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. NomegestrolAcetate 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 NomegestrolAcetate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A NomegestrolAcetate supplier is an individual or a company that provides NomegestrolAcetate active pharmaceutical ingredient (API) or NomegestrolAcetate finished formulations upon request. The NomegestrolAcetate suppliers may include NomegestrolAcetate API manufacturers, exporters, distributors and traders.
click here to find a list of NomegestrolAcetate suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 NomegestrolAcetate Drug Master File in Korea (NomegestrolAcetate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of NomegestrolAcetate. The MFDS reviews the NomegestrolAcetate KDMF as part of the drug registration process and uses the information provided in the NomegestrolAcetate KDMF to evaluate the safety and efficacy of the drug.
After submitting a NomegestrolAcetate 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 NomegestrolAcetate API can apply through the Korea Drug Master File (KDMF).
click here to find a list of NomegestrolAcetate suppliers with KDMF on PharmaCompass.
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