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
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PharmaCompass offers a list of Dimercaprol 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 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.
PharmaCompass also assists you with knowing the Dimercaprol API Price utilized in the formulation of products. Dimercaprol API Price is not always fixed or binding as the Dimercaprol Price is obtained through a variety of data sources. The Dimercaprol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A DB06782 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DB06782, including repackagers and relabelers. The FDA regulates DB06782 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DB06782 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 DB06782 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A DB06782 supplier is an individual or a company that provides DB06782 active pharmaceutical ingredient (API) or DB06782 finished formulations upon request. The DB06782 suppliers may include DB06782 API manufacturers, exporters, distributors and traders.
click here to find a list of DB06782 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 DB06782 Drug Master File in Japan (DB06782 JDMF) empowers DB06782 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 DB06782 JDMF during the approval evaluation for pharmaceutical products. At the time of DB06782 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 DB06782 suppliers with JDMF on PharmaCompass.
