QUINTA-ANALYTICA
Milan Madera has extensive experience in the field of biopharmaceutical analysis and mass spectrometry. Milan is currently serving as the Head of the QC Division at Quinta-Analytica since April 2021. Prior to this, Milan worked at Quinta Analytica s.r.o. where they held the position of Head of Dpt., Biopharmaceutical Analyses. Milan also worked as a Research Analyst at the Biopharmaceutical Analysis Department during their tenure there. Milan started their career at the National Center for Glycomics and Glycoproteomics (Indiana University) as a Mass Spec Specialist. Milan'stenure at the center lasted from April 2003 to April 2009.
Milan Madera completed their education in the field of Analytical Chemistry at Charles University in Prague. Milan first pursued a Bachelor's degree, obtaining their MSc. from 1995 to 2000. Later, they continued their academic journey at the same university, earning their Ph.D. from 2000 to 2006.
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QUINTA-ANALYTICA
Quinta is a GCP/GLP/GMP-certified, EMA and FDA-inspected European CRO offering in-house clinical testing, pharmaceutical analysis, CMC and R&D. Quinta specializes in clinical studies, bioanalytics, method development and quality control for both small and large molecules, human and veterinary IMPs as well as generics. We provide unrivaled expertise to worldwide pharmaceutical and biotechnological clients across the entire pharma spectrum. Quinta is part of the Conscio group with headquarters in Munich, Germany, laboratories in Czechia, Austria, Slovakia, Germany and offices in the USA. Our main service areas include: 1) Clinical Testing: With 2 in-house clinical units providing BE/BA/PK studies, with capacity for 60+40 beds. 2) Bioanalytical Testing: GLP/GCP solutions for preclinical & clinical studies, small & large molecules, BE/BA/PK. 3) Research & Development: Analytical R&D, impurities, extractables & leachables, degradation, trace studies. 4) Pharmaceutical Quality Control: GMP quality control, batch testing, stabilities, HAPIs, inhalation, API sourcing. 5) Microbiology: GMP sterile & non-sterile testing, microbial/water analyses, endotoxins, antibiotics & vitamins. 6) Biopharmaceutical Quality Control: GLP/GMP bioanalysis, CMC, characterizations of peptide & protein IMPs, biosimilars. Quinta was founded in 1997 and has been successfully inspected by FDA more than 10 times. Quinta is headquartered in Prague, Czech Republic.