01 1Sumitomo Chemical Co., Ltd.
01 1Japanese Pharmacopoeia afloqualone
01 1Japan
Japanese Pharmacopoeia Afloqualone
Registration Number : 217MF10077
Registrant's Address : 2-27-1 Shinkawa, Chuo-ku, Tokyo
Initial Date of Registration : 2005-05-23
Latest Date of Registration : 2007-09-06
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PharmaCompass offers a list of Metaqualone 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 Metaqualone manufacturer or Metaqualone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Metaqualone manufacturer or Metaqualone supplier.
PharmaCompass also assists you with knowing the Metaqualone API Price utilized in the formulation of products. Metaqualone API Price is not always fixed or binding as the Metaqualone Price is obtained through a variety of data sources. The Metaqualone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Metakvalon manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Metakvalon, including repackagers and relabelers. The FDA regulates Metakvalon manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Metakvalon 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 Metakvalon supplier is an individual or a company that provides Metakvalon active pharmaceutical ingredient (API) or Metakvalon finished formulations upon request. The Metakvalon suppliers may include Metakvalon API manufacturers, exporters, distributors and traders.
click here to find a list of Metakvalon 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 Metakvalon Drug Master File in Japan (Metakvalon JDMF) empowers Metakvalon 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 Metakvalon JDMF during the approval evaluation for pharmaceutical products. At the time of Metakvalon 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 Metakvalon suppliers with JDMF on PharmaCompass.
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