Webinar – Discussing Regulatory Affairs Leadership Perspectives – 2024 Survey Insights

What: Sponsored Webinar – “Discussing Regulatory Affairs Leadership Perspectives – 2024 Survey Insights”
When: Thursday, July 18th, 2024, from 10:00 AM to 11:00 AM Eastern Time (US & Canada)
Where: Online Event
How: Register Here
Why: This webinar will delve into the 2024 Survey Insights on regulatory affairs leadership, highlighting the latest trends, challenges, and opportunities in the field. Gain valuable perspectives from industry leaders and learn about the best practices to navigate the evolving regulatory landscape.

All registrants will receive a copy of the webinar recording following the live event. Register now and don’t miss out!

Join the discussion to hear from industry leaders sharing key insights and learnings from the recent survey conducted across the life sciences industry by RAPS, which had nearly 700 participants. This thought-provoking session will explore the findings and insights on topics such as top challenges and opportunities, planned investments in the near and long term, and alignment with changing technology, including real AI/Artificial Intelligence use cases.

The session will cover specifics in pharma, such as efficiency in publications and submission (including eCTD v4.0), lean authoring, readiness for IDMP, and evolving practices in medical writing. For medical devices, the session will address MDR/IVDR remediation and maintenance, QMS, and technical file management.

Our presenters will dive deeper into what these insights mean for pharma and medical device companies today and what to expect over the next two years. Participants will receive the full report complimentary, with the webinar unpacking the details and sharing the story behind the numbers, such as how life sciences companies can do more despite pressure on resources and bandwidth to stay ahead on compliance.

Register now for this unique opportunity to get the latest insights and hear from industry leaders sharing their perspectives on some of the more surprising results.

Have a question now? Submit it ahead of time and we will endeavor to provide you with a live answer during our webinar: Submit Your Question

The evolving regulatory landscape requires professionals to stay updated on the latest trends and insights to ensure compliance and strategic leadership. The 2024 Regulatory Affairs Leadership Survey provides crucial data and perspectives that can help professionals navigate these changes effectively.

Sonia Veluchamy, CEO, Co-founder, Celegence: Sonia Veluchamy brings a wealth of experience in regulatory affairs and strategic leadership. Her insights into the survey findings will shed light on the current and future state of regulatory affairs in the life sciences industry.

Punya Abbhi, COO, Co-founder, Celegence: Punya Abbhi’s extensive background in regulatory operations and strategic direction will provide valuable perspectives on how companies can leverage the survey insights to enhance their regulatory practices and maintain compliance.

Moderator: Heidi Hattendorf, Marketing Strategist in Life Sciences & Tech, Transformation Insights LLC: Heidi Hattendorf will guide the discussion, ensuring a comprehensive exploration of the survey findings and facilitating an engaging Q&A session.

• Get a pulse on the latest trends in regulatory affairs for pharma and medical devices.
• Compare top challenges, pain points, and shifts in skills, processes, and technology.
• Explore specifics on medical writing, IDMP, eCTD v4.0, document/file management systems, MDR/IVDR remediation and maintenance.
• See future investment areas related to regulatory and compliance.
• Discover real AI use cases in regulatory affairs and operations working in assistance to humans.

VPs and Directors in Regulatory Affairs, Regulatory Operations, Electronic Submissions, Medical Affairs, and Quality, as well as heads of these departments within the pharmaceutical and regulatory domain. This event is tailored for individuals seeking to enhance their understanding of the current regulatory landscape and develop strategic leadership skills.

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.

Celegence provides comprehensive regulatory outsourcing services, offering both full responsibility for regulatory deliverables and operational support. Our experienced team can help streamline your regulatory processes, ensuring compliance and efficiency. Discover how Celegence can enhance your regulatory strategy and support your success.

We look forward to sharing our insights with you during this webinar. Don’t miss this opportunity to stay ahead in the regulatory field! Register Here.