Taking Advantage of the EU MDR Delay in Uncertain Times – Webinar
Overview
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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
Associate Manager, Medical Device Services
Parvathi Nambiar
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.
Associate Manager, Medical Device Services
Kasturi Rao
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
Explore More on Systematic Literature Reviews & Compliance
AI Speeds Up Systematic Literature Reviews by 60% – Discover how AI-powered automation reduces literature review time while enhancing accuracy and efficiency.
Streamline Clinical Evaluation Report Compliance – Learn best practices for ensuring compliance with evolving CER requirements and regulatory expectations.
Authored By
Celegence Admin
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25 Apr, 2025
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