Synbias Pharma: Global Leadership in High-Potency APIs for Oncology and Specialized Therapies
01 1Gemini PharmChem Mannheim GmbH
02 1Synbias Pharma. Ltd.
03 1Nippon Microbiopharmacist Co., Ltd.
04 1Olon S. p. A.
05 1Sicor Societa (') Italiana Corticosteroidi S. r. l.
01 1Day stations epirubicin hydrochloride
02 2Epirubicin Hydrochloride
03 1Epirubicin hydrochloride
04 1Epirubicin hydrochloride "Teva"
01 2Italy
02 1Japan
03 2Switzerland
Synbias Pharma: Global Leadership in High-Potency APIs for Oncology and Specialized Therapies
Registration Number : 303MF10147
Registrant's Address : Sandhofer Strasse 96, 68305 Mannheim, Germany
Initial Date of Registration : 2021-09-09
Latest Date of Registration : 2023-02-02
Synbias Pharma: Global Leadership in High-Potency APIs for Oncology and Specialized Therapies
Registration Number : 222MF10019
Registrant's Address : Georgievskaya Str. 30a, 87515 Mariupol, Ukraine
Initial Date of Registration : 2010-01-14
Latest Date of Registration : 2010-01-14
Japanese Pharmacopoeia Epirubicin Hydrochloride
Registration Number : 223MF10127
Registrant's Address : 1-3-1 Kyobashi, Chuo-ku, Tokyo
Initial Date of Registration : 2011-08-09
Latest Date of Registration : 2022-11-16
Registration Number : 301MF10102
Registrant's Address : Strada Rivoltana Km 6/7 20090 Rodano Milano Italy
Initial Date of Registration : 2019-12-03
Latest Date of Registration : 2019-12-03
Epirubicin hydrochloride "Teva"
Registration Number : 218MF10879
Registrant's Address : Piazzale Luigi Cadorna, 4-20123 MILANO, Italy
Initial Date of Registration : 2006-11-10
Latest Date of Registration : 2006-11-10
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A Farmorubicina manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Farmorubicina, including repackagers and relabelers. The FDA regulates Farmorubicina manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Farmorubicina 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 Farmorubicina manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Farmorubicina supplier is an individual or a company that provides Farmorubicina active pharmaceutical ingredient (API) or Farmorubicina finished formulations upon request. The Farmorubicina suppliers may include Farmorubicina API manufacturers, exporters, distributors and traders.
click here to find a list of Farmorubicina 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 Farmorubicina Drug Master File in Japan (Farmorubicina JDMF) empowers Farmorubicina 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 Farmorubicina JDMF during the approval evaluation for pharmaceutical products. At the time of Farmorubicina 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 Farmorubicina suppliers with JDMF on PharmaCompass.
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