TOKYO, April 15, 2024 /PRNewswire/ — Bloomage recently effectively completed the on-site Good Manufacturing Practices (GMP) audit conducted through the Japan Pharmaceuticals and Medical Devices Agency (PMDA). As the official prescription drug regulatory firm in Japan, the PMDA has a vital duty to ensure the quality, safety, and efficacy of medical products and devices. The outcome of this audit is a testament to Bloomage’s exceptional strength in global quality management, once recognized through an authoritative body worldwide.
In addition, the company has received several foreign certifications such as ISO 9001, ISO 13485 and ISO 22000, high-level production lines that comply with the US cGMP Q7. In addition, Bloomage has achieved certifications such as CEP, DMF, KOSHER, HALAL, and VEGAN, further highlighting the wide popularity of its product quality reliability.
Bloomage’s quality control is not only evident in external certifications, but also permeates the company’s core philosophy of progress. She created the position of Quality Manager to ensure that products meet rigorous criteria from advancement to market launch.
Today, Bloomage has established five subsidiaries in the United States, France, Japan, South Korea and Singapore, with business operations covering more than 70 countries and regions around the world, delivering high quality to 4,000 pharmaceutical, medical, cosmetic and food companies. business.
Array. La company will continue to expand raw fabrics to obtain higher quality bioactive substances.
About Flowering
In 2000, Bloomage took its first steps as a manufacturer of hyaluronic acid through microbial fermentation. After more than 20 years, Bloomage has a leading global company specializing in the industrialization of hyaluronic acid. Bloomage is committed to improving people’s quality of life by creating healthier experiences.
Source: Bloomage Demonstrates Global Quality Management Excellence with On-Site Audit through Japan’s PMDA
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