Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
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01 1Pharmaceutical Works POLPHARMA S. A.
02 1Cipla Limited
03 1JUBILANT PHARMOVA LIMITED
04 1Permakem Asia Co., Ltd.
05 2Synthimed Labs Private Limited
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01 1Risedronate sodium
02 1Sodium Risedronate Hydrate
03 4Sodium risedronate hydrate
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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
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PharmaCompass offers a list of Risedronate Sodium 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 Risedronate Sodium manufacturer or Risedronate Sodium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Risedronate Sodium manufacturer or Risedronate Sodium supplier.
PharmaCompass also assists you with knowing the Risedronate Sodium API Price utilized in the formulation of products. Risedronate Sodium API Price is not always fixed or binding as the Risedronate Sodium Price is obtained through a variety of data sources. The Risedronate Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
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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