Sana-Kay Whyte-Allman
Regulatory Affairs Specialist @Tag
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WORK HISTORY
Regulatory Affairs Specialist @Tag
Toronto, ON, CA
Support MLR and creative production teams ensuring internal workflow and processes deliver the highest level of quality, compliance, and customer service.• Liaise with client contacts to develop and deploy standards and best practices to maximize quality and output of promotional and non-promotional materials.• Strategically localize global assets to ensure compliance with brand and regulatory requirements.• Manage MLR, PAAB and ASC submission of pharmaceutical promotional materials while ensuring brand and regulatory requirements.• Work closely with Medical Editors and Production team to ensure that assets are compliant to brand, style and file standards.· Therapeutic areas include hematology, respirology, diabetes, infectious diseases and vaccines, rare diseases (e.g. Pompe disease, ASMD, Fabry)
EDUCATION
North Carolina State University
Savannah River Environmental Science (Summer Program)
Johnson C. Smith University - JCSU
Bachelor of Science
University of Toronto
Doctor of Philosophy - PhD
ABOUT SANA-KAY WHYTE-ALLMAN
Regulatory affairs specialist with deep knowledge and understanding of pharmaceutical, medical and regulatory processes. My expertise spans a wide range of therapeutic areas, where I liaise with clients and cross-functional teams to strategically develop pharmaceutical promotional and educational materials, ensuring their medical accuracy and regulatory compliance. I am an excellent science communicator with over 10 years of graduate and postgraduate experience in scientific writing, editing and dissemination of medical and research related information. Overall, I am a highly motivated team-player with a strong desire to positively impact healthcare outcomes.
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