Medical Advisor

Rebecca Beausang

MSc MDRA, ISO Auditor

Rebecca Beausang is a regulatory affairs specialist with years of experience in the medical device sector. Her expertise spans regulatory compliance in major markets, including the US, EU and Asia, and the implementation of Quality Management Systems (QMS) compliant with global standards. Rebecca excels in translating complex technical information into clear, accessible content. As an active member in TOPRA & RAPS and position as Lead Auditor, she has experience in every aspect of regulatory affairs and quality assurance. Rebecca’s contributions to enhancing medical device compliance underscores her exceptional ability in providing critical medical information effectively. Follow her on Linkedin.

Education

Medical Device Regulatory Affairs, SETU – Waterford, Ireland
School of Business, MTU – Cork, Ireland
ISO Auditor Accreditation, BSI Training Academy – Cork, London, UK

Certifications

Medical Device Regulatory Affairs (MSc)
MDSAP Internal Quality Auditor
ISO 13485:2016 Lead Auditor
Bachelor of Business (B.Bus.)

Professional Accomplishments

Post-market RA enforcement for MDR submissions
ISO 13485 compliance of QMS design and implementation processes
Production site QA compliance execution
Internal auditing and engineering change analysis
Active member and contributor to TOPRA and RAPS

Accessing health and wellness information is a ubiquitous endeavor, with challenges arising in discerning trustworthy, clinically relevant, and actionable content. AdvaCare Pharma USA is dedicated to revolutionizing this scenario within the healthcare sector, providing comprehensive and accessible health information to facilitate well-informed decisions for both professionals and their patients.

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