Sponsored Webcast: AI in Action: Tech-Empowerment in Medical and Technical Writing (On Demand)
Everyone is talking about what artificial intelligence (AI) could do for pharmaceutical and medical device regulatory operations. AI for regulatory writing isn’t just a future possibility — it is happening now. Join this webcast to learn how AI cuts time, cost, and reduces the overall resource burden for pharmaceutical and medical device regulatory writing. The webcast will focus on how AI-driven solutions streamline submissions, enhance accuracy and quality, and optimize resources. You will learn of the latest practical applications from a case study and live demo. Our speakers will share real-world experience and insights on AI strategy including plans for monitoring and using AI output. This is an opportunity to see practical AI applications in action and gain actionable strategies for your own organization.
Registration Fees & Deadlines
Learning Objectives
- Practical insights on AI’s role in regulatory writing
- Key efficiencies AI brings to submission processes
- Real-world experiences from industry leaders
Who Should Attend?
- Medical Device manufacturers: Senior leaders in regulatory and clinical affairs from the medical device industry, including VPs and Directors, looking to explore AI-based solutions for streamlined compliance and data management.
- Pharmaceutical manufacturers: Senior professionals in regulatory affairs and CMC from the pharmaceutical sector, including VPs, directors, and senior managers seeking to optimize regulatory submissions with lean authoring and publishing tools.
Audience Learning Level
Intermediate: Content is designed based upon the assumption that individuals have basic knowledge of the topic(s) and/or demonstrated competence related to the topic(s). Higher-level concepts are introduced during lectures; exercises requiring synthesis and/or application of concepts are incorporated into the activity.
Higher-level concepts are introduced during lectures; exercises requiring synthesis and/or application of concepts are incorporated into the activity.
Speakers
Punya Abbhi
Chief Operating Officer and Co-Founder, Celegence
Punya is focused on tech-enabled services, including AI medical writing platform, CAPTIS®. She is highly motivated by the opportunity she sees to improve efficiency for the life sciences industry for developing regulatory strategies and global expansion.
Jason Mattis
Head Global CMC Regulatory Affairs, Kenvue
Shruti Sharma
Technical Account Manager, Celegence
Shruti Sharma is a Technical Account Manager at Celegence with a deep background in regulatory medical writing, specializing in EU MDR-compliant clinical evaluations for medical devices.
Drawing on her extensive knowledge of regulatory requirements, she translates industry needs into innovative software solutions that enhance efficiency and compliance in the Life Sciences regulatory space.
Shruti is passionate about making technology accessible and impactful, championing tech-enabled process
Dimitar Stoyanov
Director of Engineering, Celegence
Dimitar is Director of Engineering with more than 20 years of experience in the software industry. He is a result-focused individual with great track record of success stories in his past.
He has been instrumental in the successful delivery of software solutions for wide-array of industries like automotive, advertising, education, and others.
His experience in various positions and stages of the software delivery process combined with his non-compromising attitude toward the quality of the software product helps him provide valuable client solutions.
Erin Cosgrove
Vice President - Business Development - Medical DevicesDirector of Engineering, Celegence
Erin brings over 20 years of experience in medical device and diagnostics, including leadership roles at Medtronic and GE Healthcare.
She has strong expertise in helping clients leverage technology and services to grow their business by solving regulatory, quality and commercial challenges.
