Speaker for Conferences & Seminars
Embark on a journey of insightful and expert presentations tailored to meet your audience's needs. As a seasoned professional in Regulatory Affairs and Study Start-Up with over 20 years of experience in the pharmaceutical and clinical research industry, I bring a wealth of knowledge to share at your events.
Experience engaging and dynamic presentations on EU Clinical Trial Regulation, the Clinical Trial Information System (CTIS), and other regulatory affairs topics. From top-level overviews to in-depth analyses, my presentations cater to diverse audiences, ensuring valuable takeaways for participants.
Possible Presentation Titles
"Decoding EU Clinical Trial Regulation 536/2014"
Unraveling the complexities and impact on clinical trials.
"Navigating the Clinical Trial Information System (CTIS)"
A comprehensive guide to successful CTIS utilization.
"Study Start-Up: A Practical Guide for Clinical Trials"
Gain hands-on insights into overcoming regulatory challenges in clinical trial management.
“Clinical Trial Information System (CTIS) in Transitional Trials"
A comprehensive guide to successfully utilizing CTIS during the transition from CTD to CTR
Interactive Q&A Sessions
Enhance the learning experience with interactive Q&A sessions. Participants can directly engage with me, gaining deeper insights into Regulatory Affairs, Study Start-Up, and global trial management.
Flexible Delivery
Whether in-person or virtual, my speaker services adapt to the format of your event. I am equipped to deliver impactful presentations both on-site and through virtual platforms, ensuring accessibility for a diverse audience.
Book Your CTIS Expert Speaker Now
Ready to elevate your event with expert insights and engaging presentations? Book a date via Calendly or reach out via my contact form to secure my speaker services for your upcoming conference, seminar, or industry event.