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.
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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 71402_FLUKA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 71402_FLUKA, including repackagers and relabelers. The FDA regulates 71402_FLUKA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 71402_FLUKA API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A 71402_FLUKA supplier is an individual or a company that provides 71402_FLUKA active pharmaceutical ingredient (API) or 71402_FLUKA finished formulations upon request. The 71402_FLUKA suppliers may include 71402_FLUKA API manufacturers, exporters, distributors and traders.
click here to find a list of 71402_FLUKA 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 71402_FLUKA Drug Master File in Japan (71402_FLUKA JDMF) empowers 71402_FLUKA 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 71402_FLUKA JDMF during the approval evaluation for pharmaceutical products. At the time of 71402_FLUKA 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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