Board of Medical Advisors

Dolores Carrillo is a healthcare leader and licensed pharmacist with experience across the pharmaceutical supply chain. She holds a Doctor of Pharmacy (Pharm.D.) from the Faculty of Pharmacy at Complutense University of Madrid and a Master’s in Digital Business from ICEMD-ESIC. Additionally, Dolores is certified in Good Clinical Practice (GCP) and Good Distribution Practice (GDP).

Notably, Dolores has led the rapid market penetration of over 60 pharmaceutical products and implemented a strategic market access plan across 14 countries. Her work spans pharmacy operations, distribution, and manufacturing. Dr. Carrillo's clinical knowledge and unique experience has led to oversight for a broad array of products with a focus on both pharmaceuticals and medical devices. Dolores' achievements prove her commitment to quality and innovation and her pivotal roles in pharmaceutical distribution companies, laboratories, and pharmacies highlight her dedication to advancing healthcare for all. Connect with Dolores Carillo on LinkedIn to learn more.

Sandra Tashkovska is a licensed Doctor of Veterinary Medicine (DVM) and a dedicated scientific researcher specializing in animal welfare. Sandra's influential study, "Model for Identifying Appropriate Strategies for Stray Dog Population Control", has gained recognition within the veterinary community as a pivotal work driving policy change. Sandra’s academic background includes degrees from the Faculty of Veterinary Medicine at Cyril and Methodius University (Skopje, Macedonia) and the University of Zagreb (Croatia). With certifications in Positive Animal Welfare (COST Action, Slovenia), Dogs and Cats Diseases (IIEP, Poland), and Aquaculture (Bosnia and Herzegovina), Dr. Tashkovska brings a comprehensive approach to animal care and welfare.

In addition to her research, Sandra is an active participant in international conferences and workshops, including the Eastern European Regional Veterinary Conference (EERVC) in Croatia. Her work and achievements underscore a strong belief in policy awareness and strengthening best practices within the veterinary community. Connect with Sandra on Linkedin.

Rebecca Beausang is a regulatory affairs specialist with wide expertise in the medical device sector. With an MSc in Medical Device Regulatory Affairs from SETU in Ireland and certifications as an ISO 13485:2016 Lead Auditor and MDSAP Internal Quality Auditor, Rebecca ensures regulatory compliance and Quality Management Systems (QMS) across major markets, including the US, EU, and Asia. Her role as Lead Auditor and active memberships in TOPRA and RAPS highlight her in-depth knowledge in regulatory affairs and quality assurance.

Rebecca’s professional accomplishments include post-market regulatory enforcement for MDR submissions, production site QA compliance, and engineering change analysis. Rebecca's ability to translate complex regulatory information into accessible content makes her an indispensable member of any team. Connect with her on Linkedin for insights into regulatory affairs and QMS in the medical device industry.

Vanessa Atan is an accomplished healthcare professional and medical author with over 20 years of experience, combining her expertise as a Registered Nurse with a degree in Political Science to contribute to leading publications such as Biospace, Livestrong, and International Business Times. With a Nursing Licensure Certification and specialized certifications in Content Strategy, Project Management, and Generative AI, Vanessa is a trusted voice in health journalism. Her unique blend of nursing and political science backgrounds has allowed her to excel in translating complex medical information for the public.

Vanessa has contributed to the Philippines Department of Health and Livestrong, as well as serving as a content strategy team lead for the Asia region where she was tasked with managing multiple cross-functional content campaigns. Connect with Vanessa on Linkedin to explore her insights in health journalism and content strategy.