Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
01 1Pharmaceutical Works POLPHARMA S. A.
02 1Cipla Limited
03 1JUBILANT PHARMOVA LIMITED
04 1Permakem Asia Co., Ltd.
05 2Synthimed Labs Private Limited
01 1Risedronate sodium
02 1Sodium Risedronate Hydrate
03 4Sodium risedronate hydrate
01 4India
02 1Japan
03 1Poland
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
Registration Number : 222MF10015
Registrant's Address : 19 Pellinska Str. 83-200 Starogard Gdanski POLAND
Initial Date of Registration : 2010-01-07
Latest Date of Registration : 2018-10-01
Registration Number : 223MF10141
Registrant's Address : Cipla House, Peninsula Business Park, Ganpatrao Kadam Marg, Lower Parel, Mumbai - 400...
Initial Date of Registration : 2011-09-07
Latest Date of Registration : 2018-08-02
Registration Number : 302MF10157
Registrant's Address : Village-Bhagwanpur, Barwala Road, Derabassi-140 507 District-S. A. S. Nagar (Mohali)P...
Initial Date of Registration : 2020-12-23
Latest Date of Registration : 2020-12-23
Registration Number : 221MF10189
Registrant's Address : Village-Bhagwanpur, Barwala Road, Derabassi-140 507 District-S. A. S. Nagar (Mohali)P...
Initial Date of Registration : 2009-08-13
Latest Date of Registration : 2009-08-13
Registration Number : 222MF10033
Registrant's Address : 1A, Sector 16A, Noida 201 301, Uttar Pradesh, India
Initial Date of Registration : 2010-01-26
Latest Date of Registration : 2010-01-26
Registration Number : 222MF10030
Registrant's Address : 1-10-11, Nihonbashi Horidomecho, Chuo-ku, Tokyo
Initial Date of Registration : 2010-01-26
Latest Date of Registration : 2010-01-26
A Risedronate Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Risedronate Sodium, including repackagers and relabelers. The FDA regulates Risedronate Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Risedronate Sodium 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 Risedronate Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Risedronate Sodium supplier is an individual or a company that provides Risedronate Sodium active pharmaceutical ingredient (API) or Risedronate Sodium finished formulations upon request. The Risedronate Sodium suppliers may include Risedronate Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Risedronate Sodium 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 Risedronate Sodium Drug Master File in Japan (Risedronate Sodium JDMF) empowers Risedronate Sodium 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 Risedronate Sodium JDMF during the approval evaluation for pharmaceutical products. At the time of Risedronate Sodium 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 Risedronate Sodium suppliers with JDMF on PharmaCompass.
We have 5 companies offering Risedronate Sodium
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