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Report of Adverse Event Following Immunization (AEF) When completed, please send the form to your local Public Health Unit by a secure means. For more information about AEF reporting in Ontario visit
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A prospective 3-year vaccine is a type of vaccine application that outlines the development and anticipated outcomes for a vaccine over a three-year period, typically submitted to regulatory agencies for review.
Pharmaceutical companies and research organizations that are developing new vaccines must file a prospective 3-year vaccine as part of the regulatory approval process.
Filling out a prospective 3-year vaccine involves providing detailed information on the vaccine's formulation, manufacturing processes, clinical trial data, projected market impacts, and safety assessments.
The purpose of a prospective 3-year vaccine is to inform regulatory bodies about the planned development strategy for a vaccine, including timelines, objectives, and safety measures.
Information that must be reported includes the vaccine's target disease, formulation details, trial designs, risk assessments, and projected timelines for development and market entry.
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