Axplora is your partner of choice for complex APIs.
01 1Farmabios SpA@Microchem Srl@Henan Lihua Pharmaceutical Co. Ltd@Zhejiang Xianju Pharmaceutical Co. Ltd.
01 1Sam-O Pharmaceutical Co., Ltd.
01 1Fluosinonide
01 1Germany
Axplora is your partner of choice for complex APIs.
Registrant Name : Sam-O Pharmaceutical Co., Ltd.
Registration Date : 2020-05-14
Registration Number : 20200514-211-J-628
Manufacturer Name : Farmabios SpA@Microchem Srl@...
Manufacturer Address : Via Pavia 1-27027, Gropello Cairoli (PV), Italy@Via Turati, 2-29017 Fiorenzuola D'Ard...
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PharmaCompass offers a list of Fluocinonide 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 Fluocinonide manufacturer or Fluocinonide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Fluocinonide manufacturer or Fluocinonide supplier.
A Metosyn manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Metosyn, including repackagers and relabelers. The FDA regulates Metosyn manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Metosyn 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 Metosyn manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Metosyn supplier is an individual or a company that provides Metosyn active pharmaceutical ingredient (API) or Metosyn finished formulations upon request. The Metosyn suppliers may include Metosyn API manufacturers, exporters, distributors and traders.
click here to find a list of Metosyn 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 Metosyn Drug Master File in Korea (Metosyn KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Metosyn. The MFDS reviews the Metosyn KDMF as part of the drug registration process and uses the information provided in the Metosyn KDMF to evaluate the safety and efficacy of the drug.
After submitting a Metosyn 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 Metosyn API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Metosyn suppliers with KDMF on PharmaCompass.
