01 1M/s Almelo Private Limited
01 1Ziprasidone Mesilate Trihydrate EP
01 1WC-0441A3
01 1India
Ziprasidone Mesilate Trihydrate EP
Date of Issue : 2022-07-15
Valid Till : 2025-07-07
Written Confirmation Number : WC-0441A3
Address of the Firm : Unit II, Survey No. 227, 228 & 136, 137, Shabashapally (V), Shivampet (M), Medak...
A CHEBI:53757 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CHEBI:53757, including repackagers and relabelers. The FDA regulates CHEBI:53757 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CHEBI:53757 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A CHEBI:53757 supplier is an individual or a company that provides CHEBI:53757 active pharmaceutical ingredient (API) or CHEBI:53757 finished formulations upon request. The CHEBI:53757 suppliers may include CHEBI:53757 API manufacturers, exporters, distributors and traders.
click here to find a list of CHEBI:53757 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A CHEBI:53757 written confirmation (CHEBI:53757 WC) is an official document issued by a regulatory agency to a CHEBI:53757 manufacturer, verifying that the manufacturing facility of a CHEBI:53757 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting CHEBI:53757 APIs or CHEBI:53757 finished pharmaceutical products to another nation, regulatory agencies frequently require a CHEBI:53757 WC (written confirmation) as part of the regulatory process.
click here to find a list of CHEBI:53757 suppliers with Written Confirmation (WC) on PharmaCompass.
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