Dr. Markus Limberger
Dr. Markus Limberger is a co-founder and managing partner of Quasaar GmbH (established in 2015), a GMP-certified and FDA-approved contract laboratory.
Dr. Limberger earned his Ph.D. in pharmaceutical and medical chemistry at Saarland University (Degussa Fellowship, Phoenix Pharmacy Science Award 2000). Following roles in drug development, active ingredient characterization, and pharmaceutical development, he joined PHAST GmbH from 2002 to 2014. There, he played a leading role in establishing and advancing the company’s quality control and GMP departments (FDA-approved).
With over 25 years of GMP experience in the pharmaceutical industry, Dr. Limberger’s expertise lies in quality control and assurance for pharmaceuticals, biopharmaceuticals, raw materials, as well as in stability and aging studies. He is active in scientific associations and contributes as a speaker and author: APV (Quality Assurance and Quality Control expert group, pharmaceutical expert), GMP-Berater-Verlag author team.