01 1Sekisui Medical Co., Ltd.
01 1Para-hippuric acid sodium
01 1Japan
Registration Number : 217MF10775
Registrant's Address : 2-1-3 Nihonbashi, Chuo-ku, Tokyo
Initial Date of Registration : 2005-10-20
Latest Date of Registration : 2010-02-04
77
PharmaCompass offers a list of Aminohippuric Acid 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 Aminohippuric Acid manufacturer or Aminohippuric Acid supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Aminohippuric Acid manufacturer or Aminohippuric Acid supplier.
PharmaCompass also assists you with knowing the Aminohippuric Acid API Price utilized in the formulation of products. Aminohippuric Acid API Price is not always fixed or binding as the Aminohippuric Acid Price is obtained through a variety of data sources. The Aminohippuric Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Paha manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Paha, including repackagers and relabelers. The FDA regulates Paha manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Paha 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 Paha supplier is an individual or a company that provides Paha active pharmaceutical ingredient (API) or Paha finished formulations upon request. The Paha suppliers may include Paha API manufacturers, exporters, distributors and traders.
click here to find a list of Paha 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 Paha Drug Master File in Japan (Paha JDMF) empowers Paha 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 Paha JDMF during the approval evaluation for pharmaceutical products. At the time of Paha 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 Paha suppliers with JDMF on PharmaCompass.
We have 1 companies offering Paha
Get in contact with the supplier of your choice:
