Pioneering Excellence in Global Drug Information and Quality Management Solutions

Specializing in the intricate field of drug information, this company is a global leader in quality management and strategic drug development solutions. Founded in 2012, their team consists of experts who collectively bring over two decades of experience in the pharmaceutical and biotech industries. Their robust knowledge extends throughout the entire lifecycle of drug development projects, from manufacturing and pre-clinical studies to post-approval commitment trials.

With a proven track record of advisory roles with key regulatory bodies such as the FDA, EMA, NMPA, BfArM, and Swissmedic, as well as organizations including WHO, OECD, CTTI, and ACRES, the company ensures their clients stay abreast of the latest methodologies and comply with evolving regulations. Their services encompass critical areas like GMP/GDP, GLP, GPV audits across numerous global regions including the US, Europe, China, India, Japan, Southeast Asia, Australia, and South America, positioning them uniquely in the market.