Online conference on July 3, 2026 – 6:30 p.m.
How could these experimental modified mRNA substances have been injected into billions of people and trigger the greatest medical catastrophe in human history? Which government institutions in Europe and Germany failed, and how? The EMA, the Robert Koch Institute, and the Paul Ehrlich Institute are responsible for ensuring drug safety. Are they helping to bring transparency to the decision-making process, or are they instead covering things up, redacting information, and simply carrying on despite suspicions of fatalities?
More and more people no longer respect the authority of the European Commission and its EMA. Their secret backroom deals with Pfizer and the leadership’s disregard for evidence from scientists and medical associations—as well as for their own statistics on excess mortality (EUROSTAT/ECDC)—suggest that charges must be brought and that blind trust is unwarranted. According to many experts, drug safety in Europe is no longer based on evidence, but on pharmaceutical sales.
This program will document whether the legal authorities share this view and what successes or obstacles those affected and legal professionals have encountered in legal proceedings.
Speakers at the conference:
- Dr. jur. Silvia Behrendt
- EMA: Ignorance, Cover-ups, Deception, Redactions. Possible actions for EU citizens and legal professionals to demand transparency.
- Prof. Dr. Jörg Matysik and Prof. Dr. Gerald Dyker
- EMA, RKI, PEI: Chemistry professors face ignorance, cover-ups, deception, and redactions.
- Attorney Tobias Ulbrich
- Victories for vaccine-injured individuals. BioNTech and others in trouble. Federal Court of Justice refuses to go along with a cover-up justice system.
- Dr. Beate S. Pfeil
- The Bundestag’s COVID-19 Inquiry Commission and Current WHO Risks: Institutional Interdependencies, Constant Alarm?
Image: MrAronymous, CC BY-SA 4.0, via Wikimedia Commons
