01 1Sogo Pharmaceutical Co., Ltd.
01 1Chlorhexidine hydrochloride
01 1U.S.A
Registration Number : 217MF10423
Registrant's Address : 1-8-2 Marunouchi, Chiyoda-ku, Tokyo
Initial Date of Registration : 2005-08-19
Latest Date of Registration : 2021-07-20
A Chlorhexidine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Chlorhexidine Hydrochloride, including repackagers and relabelers. The FDA regulates Chlorhexidine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Chlorhexidine 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 Chlorhexidine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Chlorhexidine Hydrochloride supplier is an individual or a company that provides Chlorhexidine Hydrochloride active pharmaceutical ingredient (API) or Chlorhexidine Hydrochloride finished formulations upon request. The Chlorhexidine Hydrochloride suppliers may include Chlorhexidine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Chlorhexidine 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 Chlorhexidine Hydrochloride Drug Master File in Japan (Chlorhexidine Hydrochloride JDMF) empowers Chlorhexidine 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 Chlorhexidine Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Chlorhexidine 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 Chlorhexidine Hydrochloride suppliers with JDMF on PharmaCompass.
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