483
Maria VelinovaMaria Velinova – FDA 483, Jul 31, 2026
Record Details
An FDA inspection of Dr. Maria Velinova, a clinical investigator in Groubissen, The Netherlands, revealed a failure to conduct clinical studies in accordance with good clinical practices. The inspection found inadequate and inaccurate case histories, specifically regarding the documentation of sample processing parameters and investigational product administration for study subjects. These issues indicate significant deficiencies in record-keeping for clinical trials.
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ID · 1f1a0b24-74e5-461d-b1e8-27609bfb088e
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