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 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Clenbuterol, including repackagers and relabelers. The FDA regulates Clenbuterol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Clenbuterol 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 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Clenbuterol supplier is an individual or a company that provides Clenbuterol active pharmaceutical ingredient (API) or Clenbuterol finished formulations upon request. The Clenbuterol suppliers may include Clenbuterol API manufacturers, exporters, distributors and traders.
click here to find a list of Clenbuterol 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 Drug Master File in Japan (Clenbuterol JDMF) empowers Clenbuterol 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 JDMF during the approval evaluation for pharmaceutical products. At the time of Clenbuterol 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 suppliers with JDMF on PharmaCompass.
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