Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
01 1M/s Aarti Pharmalabs ltd
01 1Ifosfamide (Non Sterile) Ph. Eur/BP/USP
01 1WC-0099
01 1India
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Ifosfamide (Non Sterile) Ph. Eur/BP/USP
Date of Issue : 2022-08-24
Valid Till : 2025-07-29
Written Confirmation Number : WC-0099
Address of the Firm : Plot No.E-50, 50/1 and 59/1, Unit ?IV, MIDC, Tarapur?401506, Taluka: Palghar, Di...
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PharmaCompass offers a list of Ifosfamide 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 Ifosfamide manufacturer or Ifosfamide supplier for your needs.
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A Ifex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ifex, including repackagers and relabelers. The FDA regulates Ifex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ifex 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 Ifex supplier is an individual or a company that provides Ifex active pharmaceutical ingredient (API) or Ifex finished formulations upon request. The Ifex suppliers may include Ifex API manufacturers, exporters, distributors and traders.
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A Ifex written confirmation (Ifex WC) is an official document issued by a regulatory agency to a Ifex manufacturer, verifying that the manufacturing facility of a Ifex active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Ifex APIs or Ifex finished pharmaceutical products to another nation, regulatory agencies frequently require a Ifex WC (written confirmation) as part of the regulatory process.
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