01 1Hwail Pharmaceutical Co. , Ltd.
01 1Clenbuterol Hydrochloride
01 1South Korea
Registration Number : 230MF10043
Registrant's Address : 57, Jeyakgongdan 3-gil, Hyangnam-eup, Hwaseong-si, Gyeonggi-do, Korea
Initial Date of Registration : 2018-03-06
Latest Date of Registration : 2018-03-06
A Clenbuterol Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Clenbuterol Hydrochloride, including repackagers and relabelers. The FDA regulates Clenbuterol Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Clenbuterol 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 Clenbuterol Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Clenbuterol Hydrochloride supplier is an individual or a company that provides Clenbuterol Hydrochloride active pharmaceutical ingredient (API) or Clenbuterol Hydrochloride finished formulations upon request. The Clenbuterol Hydrochloride suppliers may include Clenbuterol Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Clenbuterol Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Clenbuterol Hydrochloride Drug Master File in Japan (Clenbuterol Hydrochloride JDMF) empowers Clenbuterol Hydrochloride API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Clenbuterol Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Clenbuterol Hydrochloride JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Clenbuterol Hydrochloride suppliers with JDMF on PharmaCompass.
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