01 1ERCROS S. A.
01 1Erythromycin ethyl succinate
01 1Spain
Registration Number : 225MF10104
Registrant's Address : Paseo del Deleite, s/n 28300-Aranjuez, Madrid Spain
Initial Date of Registration : 2013-05-15
Latest Date of Registration : 2021-05-13
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PharmaCompass offers a list of Erythromycin Ethyl Succinate 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 Erythromycin Ethyl Succinate manufacturer or Erythromycin Ethyl Succinate supplier for your needs.
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A MolPort-003-666-180 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-003-666-180, including repackagers and relabelers. The FDA regulates MolPort-003-666-180 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-003-666-180 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 MolPort-003-666-180 supplier is an individual or a company that provides MolPort-003-666-180 active pharmaceutical ingredient (API) or MolPort-003-666-180 finished formulations upon request. The MolPort-003-666-180 suppliers may include MolPort-003-666-180 API manufacturers, exporters, distributors and traders.
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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 MolPort-003-666-180 Drug Master File in Japan (MolPort-003-666-180 JDMF) empowers MolPort-003-666-180 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 MolPort-003-666-180 JDMF during the approval evaluation for pharmaceutical products. At the time of MolPort-003-666-180 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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