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6.4.3 Lack of Proper Testing and Approval Processes

6.4.3 Lack of Proper Testing and Approval Processes


Recommendations


The testimonies and findings from the NCI Report underscore the need for:

  1. Immediately Discontinuing Use of mRNA vaccines.

  2. Reverting to Rigorous Approval Standards: The new expedited approval processes should be revoked, and Health Canada should return to its historical safety requirements that ensure comprehensive preclinical and clinical testing before approval.

  3. Ensuring Transparency: Regulatory changes should be transparent, involving public consultation and clear communication with stakeholders, including healthcare professionals and the public.

  4. Independent Oversight: Establishing an independent body to conduct safety reviews free from industry influence is crucial for maintaining public trust and ensuring patient safety.

  5. Strengthening Post-Market Surveillance: Continuous monitoring of approved pharmaceuticals is essential to detect and address any safety concerns that may arise over time.

  6. Balancing Innovation and Safety: While promoting innovation is important, it should not compromise patient safety. Long-term effects of novel drugs must be considered, and ethical considerations should be integrated into the approval process.

Report Content Reader Page

📄 Note to Readers

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The content presented on this page has been adapted for online viewing and navigation. Due to formatting limitations within the web display system, certain elements—such as layout, spacing, and visual structure—may differ slightly from the original report.

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For the complete and fully formatted version, we encourage you to download the official PDF available on the Report Information page. The PDF reflects the report exactly as it was originally written and published.

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