01 1Sumitomo Chemical Co., Ltd.
01 1Phenothrin
01 1Japan
Registration Number : 225MF10106
Registrant's Address : 2-7-1 Nihonbashi, Chuo-ku, Tokyo
Initial Date of Registration : 2013-05-20
Latest Date of Registration : 2014-02-05
36
PharmaCompass offers a list of Phenothrin 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 Phenothrin manufacturer or Phenothrin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Phenothrin manufacturer or Phenothrin supplier.
PharmaCompass also assists you with knowing the Phenothrin API Price utilized in the formulation of products. Phenothrin API Price is not always fixed or binding as the Phenothrin Price is obtained through a variety of data sources. The Phenothrin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Sumithrin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sumithrin, including repackagers and relabelers. The FDA regulates Sumithrin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sumithrin API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Sumithrin supplier is an individual or a company that provides Sumithrin active pharmaceutical ingredient (API) or Sumithrin finished formulations upon request. The Sumithrin suppliers may include Sumithrin API manufacturers, exporters, distributors and traders.
click here to find a list of Sumithrin 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 Sumithrin Drug Master File in Japan (Sumithrin JDMF) empowers Sumithrin 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 Sumithrin JDMF during the approval evaluation for pharmaceutical products. At the time of Sumithrin 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 Sumithrin suppliers with JDMF on PharmaCompass.
We have 1 companies offering Sumithrin
Get in contact with the supplier of your choice:
