
Vernessa T. Pollard
Professional Bio
Vernessa T. Pollard advises companies on regulatory, compliance, enforcement and policy matters involving pharmaceuticals, medical devices, health information technology (HIT) and digital health solutions, services and software. She advises companies and investors on regulatory and compliance issues arising from mergers, acquisitions and other transactions involving Food and Drug Administration (FDA)-regulated products. She also counsels manufacturers, distributors and retailers on regulatory and compliance issues related to food and cosmetic marketing and safety. Read Vernessa Pollard's full bio.
FDA 2019 Year in Review
Health & Life Sciences News ·
Is Your Software a Medical Device? FDA Issues Six Digital Health Guidance Documents
Of Digital Interest ·
To Market, To Market: FDA’s Digital Health Precertification Program
Of Digital Interest ·
Reviewing Key Principles from FDA’s Artificial Intelligence White Paper
Of Digital Interest ·
FDA’s Breakthrough Device Program: Opportunities and Challenges for Device Developers
Of Digital Interest ·