HistoryBio-X Lab was established in the year of 2007. The founder, Dr. Fang-Yu Lee has over 40 years extensively experience in pharmaceutical industry. Leading his research team to apply medical technology to a new vision in functional food industry and is committed to provide most secure and safe health food products.
2007 Bio-X Lab was obtained factory registration certification to manufacture functional health supplements
2008 Relevant government plan: The application title for the Small Business Innovation Research (SBIR) from Department of Industrial Technology: The sustained release pellet form of health food supplements
2009 Certified the Good Manufacture Practice of Food
2011 Expansion of Research and Development Center was completed
2014 Introduce beverage production research equipment of Universal Can Corporation from Japan
2016 Certified the FSSC22000/HACCP Food Safety System Certification
2017 Halal Certification
Mission StatementThe Four Way Test - The Foundation of Bio-X Lab
- Is to based on sincere and faithful attitude to obtain the trust from partners and customers.
- Committed to ''quality, innovation and continuous improvement creates value to meet customer expectations'' as the quality policy. While quality and price can't be co-existence, we put quality first.
- To earn reasonable profits, provide reasonable price, to the pursuit of fair trade
- Set up coexistence and common prosperity, a strong business partnership, providing quality products and services to gain favorite from customers.
A technique in analytical chemistry used to separate, identify, and quantify each component in a mixture. It relies on pumps to pass a pressurized liquid solvent containing the sample mixture through a column filled with a solid absorbent material. Each component in the sample interacts slightly differently with the absorbent material, causing different flow rates for the different components and leading to the separation of the components as they flow out the column.
The ACQUITY UPLC System eliminates significant time and cost per sample from your analytical process while improving the quality of your results. By outperforming traditional or optimized HPLC, this technology allows chromatographers work at higher efficiency with a much wider range of linear velocities, flow rates, and back pressures.
Dissolution testing is routinely used to provide critical in vitro drug release information for both quality control purposes, i.e., to assess batch-to-batch consistency of solid oral dosage forms such as tablets, and drug development, i.e., to predict in vivo drug release profiles.
Karl Fischer Titration is a classic titration method in analytical chemistry that uses coulometric or volumetric titration to determine trace amounts of water in a sample.