Liza Soriano
Partner, Regulatory Affairs
Liza has been with Pacific BioDevelopment since 2006 as a Regulatory Affairs Associate. With a background of over eight years in Research and Development in the bio-pharmaceutical industry and academia, her experience in the drug development and discovery process spans early to late stages. She has supported project teams in the preparation, submission, maintenance and archiving of regulatory documents including INDs, BLAs, NDAs, CTAs, IMPDs, amendments, and annual reports, both domestically and internationally. Liza held a key role in the validation, maintenance and establishment of eCTD submissions using the FDA ESG in 21 CFR Part 11 compliance at Pacific BioDevelopment. She also has worked in the compiling of Due Diligence packages, including the set-up and organization of electronic and paper file systems for Regulatory, Clinical, Nonclinical and Quality documents. She holds a B.A. from the University of California at Berkeley, with a certificate in Clinical Trials Design and Management from the University of California at Santa Cruz.
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