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Advarra Consulting’s proactive, collaborative approach helps pharmaceutical, medical device and biopharmaceutical firms, as well as CROs, health systems, and academic institutions, strengthen and grow their research enterprises. With proven capabilities in GxP auditing, clinical quality assurance, regulatory affairs, vendor audits, pharmacovigilance and REMS support, SOP development and training, and research administration consulting, Advarra’s experts and global services will help your organization maintain compliance, minimize regulatory risk, and protect clinical trial participants.



Tel: +1 410.884.2900