Farmhispania Group, a leading European CDMO in HPAPI Technologies & High Potency Fermentation.
01 2FARMHISPANIA, SA
02 1Mexico City SA De CV
03 1Zhejiang Xianju Pharmaceutical Co., Ltd.
Farmhispania Group, a leading European CDMO in HPAPI Technologies & High Potency Fermentation.
Registrant Name : Hanapharmaceutical Co., Ltd.
Registration Date : 2019-11-26
Registration Number : 20190118-210-J-304(1)
Manufacturer Name : FARMHISPANIA, SA
Manufacturer Address : Passeig del Riu Besos, 9-10, 08160 MONTMELO (BARCELONA), SPAIN
Farmhispania Group, a leading European CDMO in HPAPI Technologies & High Potency Fermentation.
Registrant Name : Pami Future Co., Ltd.
Registration Date : 2019-01-18
Registration Number : 20190118-210-J-304
Manufacturer Name : FARMHISPANIA, SA
Manufacturer Address : Passeig del Riu Besos, 9-10, 08160 MONTMELO (BARCELONA), SPAIN
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PharmaCompass offers a list of Rocuronium Bromide 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 Rocuronium Bromide manufacturer or Rocuronium Bromide supplier for your needs.
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A Rocuronium Bromide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Rocuronium Bromide, including repackagers and relabelers. The FDA regulates Rocuronium Bromide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Rocuronium Bromide 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 Rocuronium Bromide supplier is an individual or a company that provides Rocuronium Bromide active pharmaceutical ingredient (API) or Rocuronium Bromide finished formulations upon request. The Rocuronium Bromide suppliers may include Rocuronium Bromide 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 Rocuronium Bromide Drug Master File in Korea (Rocuronium Bromide KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Rocuronium Bromide. The MFDS reviews the Rocuronium Bromide KDMF as part of the drug registration process and uses the information provided in the Rocuronium Bromide KDMF to evaluate the safety and efficacy of the drug.
After submitting a Rocuronium Bromide 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 Rocuronium Bromide API can apply through the Korea Drug Master File (KDMF).
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