Contact Us
"*" indicates required fields
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.
Streamline Clinical Evaluation Report Compliance – Learn best practices for ensuring compliance with evolving CER requirements and regulatory expectations.
Online Webinar
March 12, 2025 | 10:00 AM ET
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.
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.
Share
Please complete the form:
And our team will get back to you soon.