Fareva: One stop for innovative drug development, precision manufacturing and high-quality APIs.
01 1Excella GmbH & Co. K.G.
01 1Ganciclovir
01 1Luxembourg
Fareva: One stop for innovative drug development, precision manufacturing and high-quality APIs.
Registration Number : 222MF10281
Registrant's Address : NUERNBERGER STRASSE 12, 90537 FEUCHT, GERMANY
Initial Date of Registration : 2010-12-24
Latest Date of Registration : 2025-06-04
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PharmaCompass offers a list of Ganciclovir 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 Ganciclovir manufacturer or Ganciclovir supplier for your needs.
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A Ganciclovir & D5-dgA immunotoxin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ganciclovir & D5-dgA immunotoxin, including repackagers and relabelers. The FDA regulates Ganciclovir & D5-dgA immunotoxin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ganciclovir & D5-dgA immunotoxin 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 Ganciclovir & D5-dgA immunotoxin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Ganciclovir & D5-dgA immunotoxin supplier is an individual or a company that provides Ganciclovir & D5-dgA immunotoxin active pharmaceutical ingredient (API) or Ganciclovir & D5-dgA immunotoxin finished formulations upon request. The Ganciclovir & D5-dgA immunotoxin suppliers may include Ganciclovir & D5-dgA immunotoxin API manufacturers, exporters, distributors and traders.
click here to find a list of Ganciclovir & D5-dgA immunotoxin 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 Ganciclovir & D5-dgA immunotoxin Drug Master File in Japan (Ganciclovir & D5-dgA immunotoxin JDMF) empowers Ganciclovir & D5-dgA immunotoxin 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 Ganciclovir & D5-dgA immunotoxin JDMF during the approval evaluation for pharmaceutical products. At the time of Ganciclovir & D5-dgA immunotoxin 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 Ganciclovir & D5-dgA immunotoxin suppliers with JDMF on PharmaCompass.
We have 1 companies offering Ganciclovir & D5-dgA immunotoxin
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