Aarti Pharmalabs is a partner of choice for pharmaceutical companies for APIs & Intermediates. Largest Indian producer of Caffeine.
01 1M/s Aarti Pharmalabs ltd
01 1Ifosfamide Ph. Eur/BP/USP
01 1WC-0099
01 1India
Aarti Pharmalabs is a partner of choice for pharmaceutical companies for APIs & Intermediates. Largest Indian producer of Caffeine.
Date of Issue : 2025-08-22
Valid Till : 2028-08-21
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, Dis...
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A IFOSFAMIDE/MESNA KIT manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of IFOSFAMIDE/MESNA KIT, including repackagers and relabelers. The FDA regulates IFOSFAMIDE/MESNA KIT manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. IFOSFAMIDE/MESNA KIT 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 IFOSFAMIDE/MESNA KIT supplier is an individual or a company that provides IFOSFAMIDE/MESNA KIT active pharmaceutical ingredient (API) or IFOSFAMIDE/MESNA KIT finished formulations upon request. The IFOSFAMIDE/MESNA KIT suppliers may include IFOSFAMIDE/MESNA KIT API manufacturers, exporters, distributors and traders.
click here to find a list of IFOSFAMIDE/MESNA KIT suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A IFOSFAMIDE/MESNA KIT written confirmation (IFOSFAMIDE/MESNA KIT WC) is an official document issued by a regulatory agency to a IFOSFAMIDE/MESNA KIT manufacturer, verifying that the manufacturing facility of a IFOSFAMIDE/MESNA KIT active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting IFOSFAMIDE/MESNA KIT APIs or IFOSFAMIDE/MESNA KIT finished pharmaceutical products to another nation, regulatory agencies frequently require a IFOSFAMIDE/MESNA KIT WC (written confirmation) as part of the regulatory process.
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