Bloomage is a one-stop source for CEP Sodium Hyaluronate and Hyaluronic Acid// FDA-inspected & GMP-certified.
01 1Bloomage Biotechnology Corporation Limited
02 1Shandong Topscience Biotech Co., Ltd
01 2Sodium Hyaluronate
01 1SD220042
02 1SD220043
01 2China
Bloomage is a one-stop source for CEP Sodium Hyaluronate and Hyaluronic Acid// FDA-inspected & GMP-certified.
Date of Issue : 2020-07-24
Valid Till : 2025-12-18
Written Confirmation Number : SD220043
Address of the Firm : No.678 Tianchen St., High-tech Development Zone, Jinan City, Shandong Province
Topscience Biotech specializes in R&D, production, sales of Sodium Hyaluronate, focusing on Cosmetics, Medical, Pharmaceutical Grade HA
Date of Issue : 2022-12-06
Valid Till : 2025-12-18
Written Confirmation Number : SD220042
Address of the Firm : No 98, Lanshan West Road, Lanshan District, Rizhao City, Shandong Province-Post ...
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PharmaCompass offers a list of Sodium Hyaluronate 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 Sodium Hyaluronate manufacturer or Sodium Hyaluronate supplier for your needs.
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A EUFLEXXA injection manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of EUFLEXXA injection, including repackagers and relabelers. The FDA regulates EUFLEXXA injection manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. EUFLEXXA injection 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 EUFLEXXA injection written confirmation (EUFLEXXA injection WC) is an official document issued by a regulatory agency to a EUFLEXXA injection manufacturer, verifying that the manufacturing facility of a EUFLEXXA injection active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting EUFLEXXA injection APIs or EUFLEXXA injection finished pharmaceutical products to another nation, regulatory agencies frequently require a EUFLEXXA injection WC (written confirmation) as part of the regulatory process.
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