Webinar - Simplify Systematic Literature Reviews in Regulatory Compliance Using Automation & GenAI

Systematic Literature Reviews (SLRs) are essential for regulatory compliance in medical device submissions, yet they present challenges such as data complexity, evolving regulatory expectations, and resource-intensive processes. Traditional methods often lead to delays, inconsistencies, and compliance risks—but AI-powered automation can transform the way literature reviews are conducted.

In this exclusive on-demand webinar, our experts explore how automation and AI can streamline SLR workflows, enhance data accuracy, and ensure compliance with regulatory bodies like the FDA and EMA.

What You’ll Learn:

✔ How AI-driven tools can optimize systematic literature reviews and reduce manual effort
✔ Best practices for aligning literature reviews with Notified Body expectations
✔ How automation supports faster, more accurate regulatory submissions
✔ Practical insights into improving efficiency, compliance, and data management
✔ Real-world applications of AI in regulatory documentation and literature reviews

Meet the Experts

Parvathi Nambiar
Associate Manager, Medical Device Services, Celegence
Parvathi has 7+ years of experience in medical writing for regulatory affairs. She leads a team at Celegence specializing in Clinical Evaluations, Post-Market Surveillance, Clinical Investigation Plans, and Clinical Study Reports, ensuring compliance with global regulations.

Kasturi Rao
Associate Manager, Medical Device Services, Celegence
With a Ph.D. in Cancer Research and 12 years of experience in the Life Sciences industry, Kasturi has authored and reviewed key regulatory documents, including Clinical Evaluation Reports (CERs), Post-Market Surveillance (PMS) documentation, and Summary of Safety and Clinical Performance (SSCP) reports.

Who Should Watch?
🔹 Regulatory professionals handling literature reviews for medical device compliance
🔹 Medical writers and quality teams managing clinical evaluations
🔹 Regulatory affairs decision-makers seeking AI-driven compliance solutions
🔹 Medical device manufacturers looking to improve submission efficiency

Don’t Miss These Critical Insights!
Stay ahead of regulatory requirements and improve your SLR efficiency and compliance with AI-powered solutions. For expert guidance, contact us at [email protected].

Watch the webinar now and gain actionable insights into SLR automation and compliance!