01 1M/s Laurus Labs Limited
01 14-((2R,3S,4S,5R)-3-(3,4-difluoro-2-methoxyphenyl)-4,5-dimethyl-5-(trifluoromethyl)tetrahydrofuran-2-
01 1WC-0459
01 1India
4-((2R,3S,4S,5R)-3-(3,4-difluoro-2-methoxyphenyl)-4,5-dimethyl-5-(trifluoromethyl)tetrahydrofuran-2-
Date of Issue : 2022-12-02
Valid Till : 2025-11-27
Written Confirmation Number : WC-0459
Address of the Firm : Plot No. 25, 25A to 25K, Atchutapuram, Rambilli (M), Visakhapatnam-531011, Andhr...
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A HY-148800 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of HY-148800, including repackagers and relabelers. The FDA regulates HY-148800 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. HY-148800 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 HY-148800 supplier is an individual or a company that provides HY-148800 active pharmaceutical ingredient (API) or HY-148800 finished formulations upon request. The HY-148800 suppliers may include HY-148800 API manufacturers, exporters, distributors and traders.
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A HY-148800 written confirmation (HY-148800 WC) is an official document issued by a regulatory agency to a HY-148800 manufacturer, verifying that the manufacturing facility of a HY-148800 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting HY-148800 APIs or HY-148800 finished pharmaceutical products to another nation, regulatory agencies frequently require a HY-148800 WC (written confirmation) as part of the regulatory process.
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