Evonik Health Care is the innovation hub for leading life science companies
01 1Evonik Operations GmbH
01 1Dimercaprol Dimercaprol
01 1Germany
Evonik Health Care is the innovation hub for leading life science companies
Registration Number : 222MF10123
Registrant's Address : Rellinghauser Strasse 1-11 45128 Essen, Germany
Initial Date of Registration : 2010-04-05
Latest Date of Registration : 2024-06-27
81
PharmaCompass offers a list of Dimercaprol API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Dimercaprol manufacturer or Dimercaprol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dimercaprol manufacturer or Dimercaprol supplier.
A Dimersol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dimersol, including repackagers and relabelers. The FDA regulates Dimersol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dimersol 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 Dimersol supplier is an individual or a company that provides Dimersol active pharmaceutical ingredient (API) or Dimersol finished formulations upon request. The Dimersol suppliers may include Dimersol API manufacturers, exporters, distributors and traders.
click here to find a list of Dimersol suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Dimersol Drug Master File in Japan (Dimersol JDMF) empowers Dimersol 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 Dimersol JDMF during the approval evaluation for pharmaceutical products. At the time of Dimersol 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 Dimersol suppliers with JDMF on PharmaCompass.
