Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
01 1Evonik Operations GmbH
01 1Dimercaprol Dimercaprol
01 1Germany
Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
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
A Dimercaprol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dimercaprol, including repackagers and relabelers. The FDA regulates Dimercaprol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dimercaprol 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 Dimercaprol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dimercaprol supplier is an individual or a company that provides Dimercaprol active pharmaceutical ingredient (API) or Dimercaprol finished formulations upon request. The Dimercaprol suppliers may include Dimercaprol API manufacturers, exporters, distributors and traders.
click here to find a list of Dimercaprol 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 Dimercaprol Drug Master File in Japan (Dimercaprol JDMF) empowers Dimercaprol 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 Dimercaprol JDMF during the approval evaluation for pharmaceutical products. At the time of Dimercaprol 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 Dimercaprol suppliers with JDMF on PharmaCompass.
LOOKING FOR A SUPPLIER?
