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1IN THE BOARD OF COUNTY COMMISSIONERS2FOR WASHINGTON COUNTY, OREGON34In the Matter of Adopting Habitat Assessment Guidelines Pursuant to Community Development Code Section 422 (Significant Natural
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Type II and III are different types of adverse event reports that pharmaceutical companies are required to submit to regulatory agencies.
Pharmaceutical companies are required to file type II and III adverse event reports.
Type II and III adverse event reports can be filled out online through the regulatory agency's reporting portal.
The purpose of type II and III adverse event reports is to provide regulatory agencies with information on adverse events associated with pharmaceutical products.
Type II and III adverse event reports must include information about the patient, the adverse event, and the pharmaceutical product.
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