01 1Dr. Paul Lohmann GmbH & Co. KGaA
01 1Sodium citrate hydrate
01 1Germany
Registration Number : 221MF10110
Registrant's Address : Hauptstrasse 2 D-31860 Emmerthal Germany
Initial Date of Registration : 2009-06-02
Latest Date of Registration : 2009-06-02
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PharmaCompass offers a list of Trisodium Citrate Dihydrate 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 Trisodium Citrate Dihydrate manufacturer or Trisodium Citrate Dihydrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Trisodium Citrate Dihydrate manufacturer or Trisodium Citrate Dihydrate supplier.
PharmaCompass also assists you with knowing the Trisodium Citrate Dihydrate API Price utilized in the formulation of products. Trisodium Citrate Dihydrate API Price is not always fixed or binding as the Trisodium Citrate Dihydrate Price is obtained through a variety of data sources. The Trisodium Citrate Dihydrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Natriumcitrat-Dihydrat manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Natriumcitrat-Dihydrat, including repackagers and relabelers. The FDA regulates Natriumcitrat-Dihydrat manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Natriumcitrat-Dihydrat 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 Natriumcitrat-Dihydrat manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Natriumcitrat-Dihydrat supplier is an individual or a company that provides Natriumcitrat-Dihydrat active pharmaceutical ingredient (API) or Natriumcitrat-Dihydrat finished formulations upon request. The Natriumcitrat-Dihydrat suppliers may include Natriumcitrat-Dihydrat API manufacturers, exporters, distributors and traders.
click here to find a list of Natriumcitrat-Dihydrat 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 Natriumcitrat-Dihydrat Drug Master File in Japan (Natriumcitrat-Dihydrat JDMF) empowers Natriumcitrat-Dihydrat 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 Natriumcitrat-Dihydrat JDMF during the approval evaluation for pharmaceutical products. At the time of Natriumcitrat-Dihydrat JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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