Bloomage is a one-stop source for CEP Sodium Hyaluronate and Hyaluronic Acid// FDA-inspected & GMP-certified.
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01 1Bloomage Biotechnology Corporation Limited
02 1Shandong Topscience Biotech Co., Ltd
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01 2Sodium Hyaluronate
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01 1SD220042
02 1SD220043
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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, and sales of Sodium Hyaluronate, focusing on Medical and 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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sodium Hyaluronate manufacturer or Sodium Hyaluronate supplier.
PharmaCompass also assists you with knowing the Sodium Hyaluronate API Price utilized in the formulation of products. Sodium Hyaluronate API Price is not always fixed or binding as the Sodium Hyaluronate Price is obtained through a variety of data sources. The Sodium Hyaluronate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
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 supplier is an individual or a company that provides EUFLEXXA injection active pharmaceutical ingredient (API) or EUFLEXXA injection finished formulations upon request. The EUFLEXXA injection suppliers may include EUFLEXXA injection API manufacturers, exporters, distributors and traders.
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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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