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Post-Marketing Surveillance to evaluate the safety of 9-Valent Human Papillomavirus Vaccine through the Vaccine Adverse Event Reporting System (VAERS)

Trial Profile

Post-Marketing Surveillance to evaluate the safety of 9-Valent Human Papillomavirus Vaccine through the Vaccine Adverse Event Reporting System (VAERS)

Completed
Phase of Trial: Phase IV

Latest Information Update: 19 Nov 2018

At a glance

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