While many CROs can manage day-to-day operational and coordination tasks, few offer the deep regulatory insight and strategic perspective needed to drive global success. What sets us apart is our ability to combine hands-on regulatory expertise with strategic mindset - ensuring alignment with business goals, smooth collaboration across cross-functional teams, and successful Health Authority approvals worldwide. This combination of global experience, strategic execution, and regulatory depth is what truly differentiates us in a highly complex and evolving regulatory landscape. We work together with your CRO and regulatory teams to achieve success.
With over 15 years of experience in Regulatory Affairs, Margarida has led global M&A, Divestments and Clinical Development initiatives, managed complex regulatory strategies, and delivered successful outcomes across multiple markets. Her diverse background includes work with multinational pharmaceutical companies, emerging biopharma, biotech firms, CROs, and consultancies.
Recognised as a solutions-driven leader, Margarida has led high-impact projects across USA, Canada, EU, UK and Asia-Pacific and received a Global Leadership Award for leading business critical projects.
Dr. Wilkinson is a registered pharmacist, medical practitioner, and Laywer with over 20 years of experience spanning clinical medicine, pharmaceuticals, medical devices, and regulatory law. He began his career in clinical practice before moving into drug regulation at the Australian Therapeutic Goods Administration (TGA), later transitioning into the commercial medical industry in Australia.
Dr. Wilkinson has since held roles across the EU, USA, Canada, and Hong Kong, gaining extensive international experience. With a deep understanding of the medical industry across multiple jurisdictions, he brings a uniquely comprehensive perspective to every project.
