01 1M/s. Embio Ltd.,
01 1Ephedrine Sulfate USP
01 1WC-0046
01 1India
Date of Issue : 2022-09-01
Valid Till : 2025-07-28
Written Confirmation Number : WC-0046
Address of the Firm : Plot No. E-21, E-22/1, MIDC, Mahad, Dist. Raigad-402 309, Maharashtra
25
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A AKOVAZ manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AKOVAZ, including repackagers and relabelers. The FDA regulates AKOVAZ manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AKOVAZ 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 AKOVAZ supplier is an individual or a company that provides AKOVAZ active pharmaceutical ingredient (API) or AKOVAZ finished formulations upon request. The AKOVAZ suppliers may include AKOVAZ API manufacturers, exporters, distributors and traders.
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A AKOVAZ written confirmation (AKOVAZ WC) is an official document issued by a regulatory agency to a AKOVAZ manufacturer, verifying that the manufacturing facility of a AKOVAZ active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting AKOVAZ APIs or AKOVAZ finished pharmaceutical products to another nation, regulatory agencies frequently require a AKOVAZ WC (written confirmation) as part of the regulatory process.
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