QUINTA-ANALYTICA
Justyna Hofmanová is an experienced R&D Analyst at QUINTA-ANALYTICA since August 2020, focusing on research and development. Previously, Justyna served as a Research Associate at the University of Birmingham from October 2016 to July 2020, overseeing clinical research in pediatric and geriatric medicine, while also training and leading research teams. As a Teaching Assistant at the same institution, Justyna supported first-year undergraduates in their research projects. Earlier professional experience includes working as a Pharmacist at Community Pharmacy from April to September 2016, managing medication and counseling patients, and as a Research Assistant at Lek Pharmaceuticals d.d. from October 2014 to September 2015, where Justyna assisted in the preformulation department. Justyna holds a Ph.D. in Pharmacy from the University of Birmingham and a Master’s Degree in Pharmacy from the Medical University of Warsaw.
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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.