Menaka Manokaran, Lumanity

Menaka Manokaran is a seasoned expert in Regulatory and Quality, possessing extensive experience in marketing authorizations and global clinical trials for pharmaceutical drugs and medical devices. Menaka has held various positions, including Associate Director of Regulatory Affairs at Lumanity. Her expertise is particularly notable in First-in-Human studies and global Clinical Trial Authorization (CTA) submissions, highlighting her role as a subject matter expert where she has demonstrated a strong commitment to operational excellence and deliverable management for clients. Contact our strategic partner, Lumanity for help with your compliance requirements. Compliance Services: FDA 210 | FDA 211 | FDA 820 Clinical Consulting Regulatory Consulting Quality Consulting Digital Transformation Strategy Consulting Innovation and Technology Training and Development