Simplify Systematic Literature Reviews in Regulatory Compliance Using AI

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.

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

Webinar Speakers

  • Parvathi Nambiar, Associate Manager, Medical Device Services
    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
    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.

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

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

Explore More on Systematic Literature Reviews & Compliance

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