Arete-Zoe, LLC

healthcare medical devices arete-zoe medicine veronika valdova clinical trials pharmacovigilance drug safety clinical studies clinical research pharmaceutical industry essential medicines data analysis risk management clinical evaluation drug shortages healthcare systems health pharmaceuticals post-market surveillance eu mdr ibm watson pmcf czech medical device regulation post-market clinical follow-up health systems stem cells vaccine mdr 2017/745 medical technology regenerative medicine sexual assault hipaa supply chain security vaccine safety side effects clinical trial registry product labeling workshop scientific literature medical equipment covid-19 patient injury globalization clinical investigations medical ethics patient confidentiality availability of medicines sepsis data security biomedical research supply chain distribution chain supply chain terrorism training european regulations generics czech republic medicines who eml regulatory requirements combination products drug-device combination isop date rape rape date rape drugs civil rights medical countermeasures dual-use of biotechnology hospital vulnerable populations cost of treatment pricing data breach pediatric medication medication errors cpoe signal detection causality assessment case processing literární rešerše biologické hodnocení psur klinická dokumentace klinické hodnocení zdravotnické prostředky vaccine label comirnaty tozinameran warnings and precautions adverse reactions adverse events mrna vaers explorer anthrax immunization prevention vaersexplorer adenovirus sodium oxybate warfarin rosiglitazone paroxetine olanzapine mefloquine isotretinoin gemtuzumab ozogamicin market withdrawal drug withdrawal research pharmacovigilance database case study product withdrawal ethics committee assisted suicide gerontology end of life care case report patient history clinical guidelines privacy lifestyle childhood obesity medical oaths environmental biocompatibility assessment re eu legislation medical device manufacturing coronavirus real world evidence heath women's health pharma mdr safety data exchange agreements infectious diseases sexually transmitted diseases biotech criminal justice hungary gastrointestinal tract patient safety aids hiv tuberculosis antibiotics antiinfectives post-authorization surveillance precision medicine cancer oncology adverse drug reaction adverse drug event drug overdose opioids opioid crisis gdp gmp gcp gxp gvp personal data protection eu data privacy directive data integrity biologics study endpoints interventional studies who country study behavioral studies state institute for drug control business intelligence market analysis systems approach to training professional education addie information processing evidence generation cgtp information information environment investigations police response security activism 1080 business competition ecoterrorism 1080 poison risk control drug development stamp system theoretic accident modeling and processes systems approach solution development internal validity bias medical literature biomedical literature cognitive traps medical research validity assessment external valididty literature review source evaluation