Discussing Regulatory Affairs: Leadership Perspectives & 2024 Survey Insights - Webinar скачать в хорошем качестве

Discussing Regulatory Affairs: Leadership Perspectives & 2024 Survey Insights - Webinar

Join the discussion to hear from industry leaders sharing key insights and learnings from the recent survey conducted across the life sciences industry from Celegence in partnership with RAPS which had nearly 700 participants. This will be a thought-provoking session exploring the findings and insights on topics such as top challenges and opportunities, planned investments near and long term, and alignment to changing technology such as real AI/Artificial Intelligence use cases. The session will look at specifics in pharma such as efficiency in publications and submission including eCTD v4.0 (electronic common technical document), lean authoring, readiness for IDMP (identification of medicinal products), and evolving practices in medical writing. On medical devices, the session will cover specifics such as MDR/IVDR remediation and maintenance, QMS, and technical file management. Our presenters will dive deeper into what this means for pharma and medical device companies today and what to expect over the next two years. Webinar Speakers: Sonia Veluchamy, CEO, CEO, Co-founder, Celegence Punya Abbhi, COO, Co-founder, Celegence Moderator: Heidi Hattendorf, Marketing Strategist in Life Sciences & Tech, Transformation Insights LLC Unlock actionable insights with our webinar focusing on key learning objectives: 1. Get a pulse on the latest trends in regulatory affairs for pharma and medical devices 2. Compare top challenges, pain points and shifts in skills, process and technology 3. Explore specifics on medical writing, IDMP, eCTD v4.0, document/file management systems, MDR/IVDR remediation and maintenance 4. See future investment areas related to regulatory and compliance 5. Discover real AI use cases in regulatory affairs and operations working in assistance to humans Celegence can simplify your compliance journey with consulting services and technology enabled solutions that are tailored to the evolving needs of Life Science organizations. Through our guidance and technology-enabled services, you can leverage our global expertise and robust regulatory intelligence, to support your product lifecycle management and submission strategies. For further regulatory assistance or queries on how Celegence can support your organization, reach out to info@celegence.com today.