Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.
01 1EGIS PHARMACEUTICALS PRIVATE LIMITED COMPANY
02 1Cheer Fine Pharmaceutical Co. , Ltd.
03 2Daiwa Pharmaceutical Industries Co., Ltd.
04 1Harman Finochem Ltd.
05 1Indoco Remedies Limited
06 2Sicor Societa (') Italiana Corticosteroidi S. r. l.
07 1Tianish Laboratories Private Limited
08 1Zhejiang Huayang Pharmaceutical Co., Ltd.
Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.
Registration Number : 231MF10077
Registrant's Address : H-1106 BUDAPEST KERESZTURI UT 30-38 HUNGARY
Initial Date of Registration : 2019-03-29
Latest Date of Registration : 2019-03-29
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PharmaCompass offers a list of Allopurinol 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 Allopurinol manufacturer or Allopurinol supplier for your needs.
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A Milurit manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Milurit, including repackagers and relabelers. The FDA regulates Milurit manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Milurit 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 Milurit supplier is an individual or a company that provides Milurit active pharmaceutical ingredient (API) or Milurit finished formulations upon request. The Milurit suppliers may include Milurit 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 Milurit Drug Master File in Japan (Milurit JDMF) empowers Milurit 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 Milurit JDMF during the approval evaluation for pharmaceutical products. At the time of Milurit 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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