01 1Janssen Pharmaceutical Sciences Unlimited Company
01 1Korea Janssen Co., Ltd.
01 1Rilpivirine hydrochloride
01 1U.S.A
Registrant Name : Korea Janssen Co., Ltd.
Registration Date : 2011-10-28
Registration Number : Su217-14-ND
Manufacturer Name : Janssen Pharmaceutical Scien...
Manufacturer Address : Little Island Industrial EST., Little Island, Co. Cork, Ireland_x000D_
A Rilpivirine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Rilpivirine Hydrochloride, including repackagers and relabelers. The FDA regulates Rilpivirine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Rilpivirine Hydrochloride 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 Rilpivirine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Rilpivirine Hydrochloride supplier is an individual or a company that provides Rilpivirine Hydrochloride active pharmaceutical ingredient (API) or Rilpivirine Hydrochloride finished formulations upon request. The Rilpivirine Hydrochloride suppliers may include Rilpivirine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Rilpivirine Hydrochloride 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 Rilpivirine Hydrochloride Drug Master File in Korea (Rilpivirine Hydrochloride KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Rilpivirine Hydrochloride. The MFDS reviews the Rilpivirine Hydrochloride KDMF as part of the drug registration process and uses the information provided in the Rilpivirine Hydrochloride KDMF to evaluate the safety and efficacy of the drug.
After submitting a Rilpivirine Hydrochloride 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 Rilpivirine Hydrochloride API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Rilpivirine Hydrochloride suppliers with KDMF on PharmaCompass.
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