Risedronate (sodium) | API EU Written Confirmation | WC

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Axplora

Germany

IMCAS World Congress

Not Confirmed

Axplora- The partner of choice for complex APIs.

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Germany

Virtual Booth

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Risedronate Sodium (Hemipentahydrate)USP

Date of Issue : 2022-03-18

Valid Till : 2025-05-28

Written Confirmation Number : WC-0019

Address of the Firm : Plot No. 115, Ramky Pharma City, SEZ, Parawada Mandal, Visakhapatnam, Andhra Pra...

Product Web Link

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Ind Swift Laboratories Limited

India

IMCAS World Congress

Not Confirmed

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Macleods Pharmaceuticals Limited

India

IMCAS World Congress

Not Confirmed

10

Sun Pharmaceutical Industries Limited

India

IMCAS World Congress

Not Confirmed

Risedronate (sodium) Manufacturers

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.

Risedronate (sodium) Suppliers

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.

Risedronate (sodium) WC

A Risedronate (sodium) written confirmation (Risedronate (sodium) WC) is an official document issued by a regulatory agency to a Risedronate (sodium) manufacturer, verifying that the manufacturing facility of a Risedronate (sodium) active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Risedronate (sodium) APIs or Risedronate (sodium) finished pharmaceutical products to another nation, regulatory agencies frequently require a Risedronate (sodium) WC (written confirmation) as part of the regulatory process.

click here to find a list of Risedronate (sodium) suppliers with Written Confirmation (WC) on PharmaCompass.

Risedronate (sodium) Manufacturers | Traders | Suppliers

We have 11 companies offering Risedronate (sodium)

Get in contact with the supplier of your choice:

Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.