EMA Roadmap Update: PMS Capabilities and the End of the Legacy Era
Danielle W. Marcelli
10 Mar, 2026
Danielle brings over 26 years of experience in Regulatory Affairs and Operations, Clinical Compliance, and Label Management across the Pharmaceutical and Medical Device industries, with expertise in strategic relationship management.
Her experience includes providing Regulatory Information Management, Trial Master File and SPL, Product Monograph, FHIR & UDI solutions to the Life Sciences industry.
Danielle holds a B.A. from The George Washington University. With her industry experience, Danielle contributes strong account management expertise and aligns unmet industry needs with company growth goals.
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