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HOME
ABOUT
SERVICES
Medical Devices EU
EU MDR 2017/745
Zdravotnické prostředky (CZ)
Research
Training
Operational Risk Management
LIBRARY
Wound irrigation PMCF study (2025)
The Dark Side of Pharma Globalization (2021)
Drug Safety Surveillance (2018)
Essential Medicines CZ-HU (2017)
Hospital Risk Series (2017)
BW (2017)
Sexual assault/STDs (2017)
Pharma Supply Chain (2016)
Global Pharma Primer (2015)
Women's Medicines (2015)
Survival Guide to Stem Cells (2015)
EVENTS
ISoP SIG Medical devices 2024
WDSEC 2023
Clinical Evaluation Workshop 2023
PV Workshop 2022
PV Workshop 2019
Medical device workshops
VAERS Explorer
Resources
Vaccine-Labels
Adenovirus vaccine
Anthrax vaccine
Medical Ethics
The Oath of Hippocrates
The Oath of Maimonides
The Percival Code
AMA Code of Medical Ethics
Prussian Directive
Reich's Guidelines
The Nuremberg Code
The Declaration of Geneva
WMA International Code of Medical Ethics
The Lasagna Oath
The Declaration of Helsinki
AHA's Patient Bill of Rights
The Belmont Report
European Charter of Medical Ethics
Current U.S. Regulations
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Blog
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Medical device workshops
Clinical evaluation: Applicable standards
Supporting medical device product life-cycle
Clinical evaluation: Supporting medical device product life-cycle. Applicable Standards
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Clinical documentation for medical devices
Medical Device Regulation (EU) 2017/745
Clinical documentation for medical devices
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