[FREE WEBINAR] The Art of State of The Art: All You Need to Know

By: Sarah VanVickle Chaves, Director of IVD and Scientific Writing Services, Ph.D. Molecular and Cellular Biology

View Criterion Edge’s President, Laurie Mitchell, and Evidence Partners’ President, Peter O’Blenis, for an xTalks webinar on State of the Art Literature Review: How To Get It Right. (recorded: December 11, 2018, 9 AM PST/12pm EST)

Tune in to learn about key components of an effective state of the art description as well as common points of failure in state of the art literature reviews. Peter and Laurie will expand on sound methods and expert tips for completing an effective literature search. They will be covering the best practices to efficiently produce and maintain a fully compliant and audit-ready clinical background/state of the art description using DistillerSR, and addressing any questions or concerns that may arise.

Those working in Regulatory Affairs, Quality Assurance, Clinical Evaluation and Clinical Affairs, as well as Medical Writers are invited to the discussion of best practices and tools to produce fully compliant state of the art literature reviews.

Both Peter and Laurie each bring rich knowledge to the discussion.

Peter O’Blenis is a pioneer in literature review automation, Peter has worked with over 250 research groups around the globe since 2001 and has published extensively on best practices and methodologies for using technology to improve the review process.

Laurie Mitchell, Founder and President of Criterion Edge, has over 25 years of experience in clinical research, primarily in medical writing, pharmacovigilance management, and regulatory reporting. Having worked for three of the four major medical device sponsors, she maintains expertise across many therapeutic areas.

The presentation will be followed by Q&A for attendee discussion and participation. The webinar is sponsored by xTalks, Evidence Partners and Criterion Edge.

TALK TO AN EXPERT

Whether you’re navigating a complex regulatory submission, preparing for an audit, or simply exploring outsourced support — our team is here to help.

Criterion Edge specializes in high-quality, compliant medical writing services for the life sciences industry. Use the form to tell us a bit about your needs — one of our experts will follow up within one business day.

Need a faster response? Use the chat icon in the lower-right corner to speak with us immediately during business hours.

  • No obligation — just an open conversation
  • Expert guidance from PhD-level writers
  • Trusted by leading MedTech & Pharma companies
  • Fast turnaround for time-sensitive projects
  • Clear quotes and scoping available

How Can We Help?

TALK TO AN EXPERT

Whether you’re navigating a complex regulatory submission, preparing for an audit, or simply exploring outsourced support — our team is here to help.

Criterion Edge specializes in high-quality, compliant medical writing services for the life sciences industry. Use the form to tell us a bit about your needs — one of our experts will follow up within one business day.

Need a faster response? Use the chat icon in the lower-right corner to speak with us immediately during business hours.

  • No obligation — just an open conversation
  • Expert guidance from PhD-level writers
  • Trusted by leading MedTech & Pharma companies
  • Fast turnaround for time-sensitive projects
  • Clear quotes and scoping available

How Can We Help?

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UPCOMING WEBINAR: Beyond AI: Why the Future of Scientific and Regulatory Writing Is Human + AI · October 28 · 8 AM PDT · 10 AM CDT · 11 AM EDT

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